TITLE I GENERAL ISSUES
Article 1 Purpose and scope
1.F1The purpose of this Regulation is to ensure a high level of protection of human health and the environment ... by:
(a)[F2 establishingF2] the criteria for classification of substances and mixtures, and the rules on labelling and packaging for hazardous substances and mixtures;
(b)providing an obligation for:
manufacturers, importers and downstream users to classify substances and mixtures placed on the market;
suppliers to label and package substances and mixtures placed on the market;
manufacturers, producers of articles and importers to classify those substances not placed on the market that are subject to registration or notification under Regulation (EC) No 1907/2006;
(c)providing an obligation for manufacturers and importers of substances to notify the Agency of such classifications and label elements if these have not been submitted to the Agency as part of a registration under Regulation (EC) No 1907/2006;
(d)establishing a list of substances with their [F3mandatory classifications and labelling elements in the GB mandatory classification and labelling listF3] ;
F4(e). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2.This Regulation shall not apply to the following:
(a)radioactive substances and mixtures within the scope of [F5the Ionising Radiations Regulations 2017F5] laying down basic safety standards for the protection of the health of workers and the general public against the danger arising from ionising radiation;
(b)substances and mixtures which are subject to customs supervision, provided that they do not undergo any treatment or processing, and which are in temporary storage, or in a free zone or free warehouse with a view to re-exportation, or in transit;
(c)non-isolated intermediates;
(d)F6substances and mixtures for scientific research and development, which are not placed on the market, provided they are used under controlled conditions in accordance with ... workplace and environmental legislation.
3.Waste as defined in [F7Directive 2008/98/EC of the European Parliament and of the Council of 19 November 2008F7] on waste is not a substance, mixture or article within the meaning of Article 2 of this Regulation.
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5.This Regulation shall not apply to substances and mixtures in the following forms, which are in the finished state, intended for the final user:
(a)medicinal products as defined in [F9the Human Medicines Regulations 2012F9] ;
(b)veterinary medicinal products as defined in [F10the Veterinary Medicines Regulations 2013F10] ;
(c)cosmetic products as defined in [F11Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic productsF11] ;
[F12 (d)medical devices as defined in the Medical Devices Regulations 2002 which are invasive or used in direct physical contact with the human body, and in vitro diagnostic medical devices, as defined in the same regulations.F12]
(e)food or feeding stuffs as defined in Regulation (EC) No 178/2002 including when they are used:
as a food additive in foodstuffs within the scope of [F13Regulation (EC) No 1333/2008 of the European Parliament and of the Council of 16 December 2008 on food additivesF13] ;
as a flavouring in foodstuffs within the scope of [F14Regulation (EC) No 1334/2008 of the European Parliament and of the Council of 16 December 2008 on flavourings and certain food ingredients with flavouring properties for use in and on foods F15...F14] ;
as an additive in feeding stuffs within the scope of Regulation (EC) No 1831/2003;
in animal nutrition within the scope of [F16Regulation (EC) No 767/2009 of the European Parliament and of the Council of 13 July 2009 on the placing on the market and use of feedF16] .
6.Save where Article 33 applies this Regulation shall not apply to the transport of dangerous goods by air, sea, road, rail or inland waterways.
Article 2 Definitions
For the purpose of this Regulation, the following definitions shall apply:
‘hazard class’ means the nature of the physical, health or environmental hazard;
‘hazard category’ means the division of criteria within each hazard class, specifying hazard severity;
‘hazard pictogram’ means a graphical composition that includes a symbol plus other graphic elements, such as a border, background pattern or colour that is intended to convey specific information on the hazard concerned;
‘signal word’ means a word that indicates the relative level of severity of hazards to alert the reader to a potential hazard; the following two levels are distinguished:
‘Danger’ means a signal word indicating the more severe hazard categories;
‘Warning’ means a signal word indicating the less severe hazard categories;
‘hazard statement’ means a phrase assigned to a hazard class and category that describes the nature of the hazards of a hazardous substance or mixture, including, where appropriate, the degree of hazard;
‘precautionary statement’ means a phrase that describes recommended measure(s) to minimise or prevent adverse effects resulting from exposure to a hazardous substance or mixture due to its use or disposal;
‘substance’ means a chemical element and its compounds in the natural state or obtained by any manufacturing process, including any additive necessary to preserve its stability and any impurity deriving from the process used, but excluding any solvent which may be separated without affecting the stability of the substance or changing its composition;
‘mixture’ means a mixture or solution composed of two or more substances;
‘article’ means an object which during production is given a special shape, surface or design which determines its function to a greater degree than does its chemical composition;
[F17 “producer of an article” means any natural or legal person—
who makes or assembles an article within Great Britain;
who makes or assembles an article within Northern Ireland which is a qualifying Northern Ireland good and which is placed directly on the market in Great Britain;F17]
‘polymer’ means a substance consisting of molecules characterised by the sequence of one or more types of monomer units. Such molecules must be distributed over a range of molecular weights wherein differences in the molecular weight are primarily attributable to differences in the number of monomer units. A polymer comprises the following:
a simple weight majority of molecules containing at least three monomer units which are covalently bound to at least one other monomer unit or other reactant;
less than a simple weight majority of molecules of the same molecular weight.
In the context of this definition a ‘monomer unit’ means the reacted form of a monomer substance in a polymer;
‘monomer’ means a substance which is capable of forming covalent bonds with a sequence of additional like or unlike molecules under the conditions of the relevant polymer-forming reaction used for the particular process;
‘registrant’ means the manufacturer or the importer of a substance or the producer or importer of an article submitting a registration for a substance under Regulation (EC) No 1907/2006 ;
‘manufacturing’ means production or extraction of substances in the natural state;
[F18 “manufacturer” means any natural or legal person—
established in Great Britain, who manufactures a substance within Great Britain;
established in Northern Ireland, who manufactures a substance which is a qualifying Northern Ireland good and which is placed directly on the market in Great Britain;F18]
[F19 “import” means the physical introduction into Great Britain, except where the goods are qualifying Northern Ireland goods; F19]
[F20 “importer” means any natural or legal person established within Great Britain who is responsible for import; F20]
‘placing on the market’ means supplying or making available, whether in return for payment or free of charge, to a third party. Import shall be deemed to be placing on the market;
‘downstream user’ means any natural or legal person established [F21 within Great Britain, or within Northern Ireland in the case of qualifying Northern Ireland goods which are placed directly on the market in Great Britain F21] , other than the manufacturer or the importer, who uses a substance, either on its own or in a mixture, in the course of his industrial or professional activities. A distributor or a consumer is not a downstream user. A re-importer exempted pursuant to Article 2(7)(c) of Regulation (EC) No 1907/2006 shall be regarded as a downstream user;
‘distributor’ means any natural or legal person established [F22 within Great Britain, or within Northern Ireland in the case of qualifying Northern Ireland goods which are placed directly on the market in Great Britain F22] , including a retailer, who only stores and places on the market a substance, on its own or in a mixture, for third parties;
‘intermediate’ means a substance that is manufactured for and consumed in or used for chemical processing in order to be transformed into another substance (hereinafter referred to as ‘synthesis’);
‘non-isolated intermediate’ means an intermediate that during synthesis is not intentionally removed (except for sampling) from the equipment in which the synthesis takes place. Such equipment includes the reaction vessel, its ancillary equipment, and any equipment through which the substance(s) pass(es) during a continuous flow or batch process as well as the pipework for transfer from one vessel to another for the purpose of the next reaction step, but it excludes tanks or other vessels in which the substance(s) are stored after the manufacture;
‘the Agency’ means the [F23 Health and Safety Executive F23] ;
‘competent authority’ means the authority or authorities or bodies [F24 appointed to carry out the obligations arising from this Regulation by the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013 F24] ;
‘use’ means any processing, formulation, consumption, storage, keeping, treatment, filling into containers, transfer from one container to another, mixing, production of an article or any other utilisation;
‘supplier’ means any manufacturer, importer, downstream user or distributor placing on the market a substance, on its own or in a mixture, or a mixture;
‘alloy’ means a metallic material, homogeneous on a macroscopic scale, consisting of two or more elements so combined that they cannot be readily separated by mechanical means; alloys are considered to be mixtures for the purposes of this Regulation;
‘UN RTDG’ means the United Nations Recommendations on the Transport of Dangerous Goods;
‘notifier’ means the manufacturer or the importer, or group of manufacturers or importers notifying to the Agency;
‘scientific research and development’ means any scientific experimentation, analysis or chemical research carried out under controlled conditions;
‘cut-off value’ means a threshold of any classified impurity, additive or individual constituent in a substance or in a mixture, above which threshold these shall be taken into account for determining if the substance or the mixture, respectively, shall be classified;
‘concentration limit’ means a threshold of any classified impurity, additive or individual constituent in a substance or in a mixture that may trigger classification of the substance or the mixture, respectively;
‘differentiation’ means distinction within hazard classes depending on the route of exposure or the nature of the effects;
‘M-factor’ means a multiplying factor. It is applied to the concentration of a substance classified as hazardous to the aquatic environment acute category 1 or chronic category 1, and is used to derive by the summation method the classification of a mixture in which the substance is present;
‘package’ means the complete product of the packing operation, consisting of the packaging and its contents;
‘packaging’ means one or more receptacles and any other components or materials necessary for the receptacles to perform their containment and other safety functions;
‘intermediate packaging’ means packaging placed between inner packaging, or articles, and outer packaging.
[F25 “GB mandatory classification and labelling list” means the list of mandatory classification and labelling requirements of substances and groups of substances established and maintained in accordance with Article 38A;
F26 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
“European Chemicals Agency” means the Agency established by Article 75 of Regulation (EC) No 1907/2006 as it has effect in EU law;
“EU CLP Regulation” means Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EEC , and amending Regulation (EC) No 1907/2006 , as it has effect in EU law;
“Devolved Authority” means—
the Scottish Ministers, or
the Welsh Ministers;
“qualifying Northern Ireland goods” has the meaning given by regulations made under section 8C(6) of the European Union (Withdrawal) Act 2018 . F25]
Article 3 Hazardous substances and mixtures and specification of hazard classes
A substance or a mixture fulfilling the criteria relating to physical hazards, health hazards or environmental hazards, laid down in Parts 2 to 5 of Annex I is hazardous and shall be classified in relation to the respective hazard classes provided for in that Annex.
Where, in Annex I, hazard classes are differentiated on the basis of the route of exposure or the nature of the effects, the substance or mixture shall be classified in accordance with such differentiation.
Article 4 General obligations to classify, label and package
1.Manufacturers, importers and downstream users shall classify substances or mixtures in accordance with Title II before placing them on the market.
2.Without prejudice to the requirements of paragraph 1, manufacturers, producers of articles and importers shall classify those substances not placed on the market in accordance with Title II where:
(a)Articles 6, 7(1) or (5), 17 or 18 of Regulation (EC) No 1907/2006 provide for registration of a substance;
(b)Articles 7(2) or 9 of Regulation (EC) No 1907/2006 provide for notification.
3.If a substance is subject to [F27mandatoryF27] classification and labelling in accordance with Title V through an entry in [F28the GB mandatory classification and labelling listF28] , that substance shall be classified in accordance with that entry, and a classification of that substance in accordance with Title II shall not be performed for the hazard classes or differentiations covered by that entry.
However, where the substance also falls within one or more hazard classes or differentiations not covered by an entry in [F29the GB mandatory classification and labelling listF29] , classification under Title II shall be carried out for those hazard classes or differentiations.
4.Where a substance or mixture is classified as hazardous, suppliers shall ensure that the substance or mixture is labelled and packaged in accordance with Titles III and IV, before placing it on the market.
5.In fulfilling their responsibilities under paragraph 4, distributors [F30who are established within Great BritainF30] may use the classification for a substance or mixture derived in accordance with Title II by an actor in the supply chain.
6.In fulfilling their responsibilities under paragraphs 1 and 4, downstream users[F31 who are established within Great BritainF31] may use the classification of a substance or mixture derived in accordance with Title II by an actor in the supply chain, provided that they do not change the composition of the substance or mixture.
7.A mixture referred to in Part 2 of Annex II that contains any substance classified as hazardous shall not be placed on the market, unless it is labelled in accordance with Title III.
8.For the purposes of this Regulation, the articles referred to in section 2.1 of Annex I shall be classified, labelled and packaged in accordance with the rules for substances and mixtures before being placed on the market.
9.Suppliers in a supply chain shall cooperate to meet the requirements for classification, labelling and packaging in this Regulation.
10.Substances and mixtures shall not be placed on the market unless they comply with this Regulation.
TITLE II HAZARD CLASSIFICATION
CHAPTER 1 Identification and examination of information
Article 5 Identification and examination of available information on substances
1.Manufacturers, importers and downstream users of a substance shall identify the relevant available information for the purposes of determining whether the substance entails a physical, health or environmental hazard as set out in Annex I, and, in particular, the following:
(a)data generated in accordance with any of the methods referred to in Article 8(3);
(b)epidemiological data and experience on the effects on humans, such as occupational data and data from accident databases;
(c)any other information generated in accordance with section 1 of Annex XI to Regulation (EC) No 1907/2006;
(d)any new scientific information;
(e)any other information generated under internationally recognised chemical programmes.
The information shall relate to the forms or physical states in which the substance is placed on the market and in which it can reasonably be expected to be used.
2.Manufacturers, importers and downstream users shall examine the information referred to in paragraph 1 to ascertain whether it is adequate, reliable and scientifically valid for the purpose of the evaluation pursuant to Chapter 2 of this Title.
Article 6 Identification and examination of available information on mixtures
1.Manufacturers, importers and downstream users of a mixture shall identify the relevant available information on the mixture itself or the substances contained in it for the purposes of determining whether the mixture entails a physical, health or environmental hazard as set out in Annex I, and, in particular, the following:
(a)data generated in accordance with any of the methods referred to in Article 8(3) on the mixture itself or the substances contained in it;
(b)epidemiological data and experience on the effects on humans for the mixture itself or the substances contained in it, such as occupational data or data from accident databases;
(c)any other information generated in accordance with section 1 of Annex XI to Regulation (EC) No 1907/2006 for the mixture itself or the substances contained in it;
(d)any other information generated under internationally recognised chemical programmes for the mixture itself or the substances contained in it.
The information shall relate to the forms or physical states in which the mixture is placed on the market and, when relevant, in which it can reasonably be expected to be used.
2.Subject to paragraphs 3 and 4, where the information referred to in paragraph 1 is available for the mixture itself, and the manufacturer, importer or downstream user has ascertained that information to be adequate and reliable and where applicable, scientifically valid, that manufacturer, importer or downstream user shall use that information for the purposes of the evaluation pursuant to Chapter 2 of this Title.
3. For the evaluation of mixtures pursuant to Chapter 2 of this Title in relation to the ‘germ cell mutagenicity’, ‘carcinogenicity’ and ‘reproductive toxicity’ hazard classes referred to in sections 3.5.3.1, 3.6.3.1 and 3.7.3.1 of Annex I, the manufacturer, importer or downstream user shall only use the relevant available information referred to in paragraph 1 for the substances in the mixture.
Further, in cases where the available test data on the mixture itself demonstrate germ cell mutagenic, carcinogenic or toxic to reproduction effects which have not been identified from the information on the individual substances, those data shall also be taken into account.
4. For the evaluation of mixtures pursuant to Chapter 2 of this Title in relation to the ‘biodegradation and bioaccumulation’ properties within the ‘hazardous to the aquatic environment’ hazard class referred to in sections 4.1.2.8 and 4.1.2.9 of Annex I, the manufacturer, importer or downstream user shall only use the relevant available information referred to in paragraph 1 for the substances in the mixture.
5.Where no or inadequate test data on the mixture itself of the kind referred to in paragraph 1 are available, the manufacturer, importer or downstream user shall use other available information on individual substances and similar tested mixtures which may also be considered relevant for the purposes of determining whether the mixture is hazardous, provided that that manufacturer, importer or downstream user has ascertained that information to be adequate and reliable for the purpose of the evaluation pursuant to Article 9(4).
Article 7 Animal and human testing
1.Where new tests are carried out for the purposes of this Regulation, tests on animals [F32to which the Animals (Scientific Procedures) Act 1986 appliesF32] shall be undertaken only where no other alternatives, which provide adequate reliability and quality of data, are possible.
2.Tests on non-human primates shall be prohibited for the purposes of this Regulation.
3.Tests on humans shall not be performed for the purposes of this Regulation. Data obtained from other sources, such as clinical studies, can however be used for the purposes of this Regulation.
Article 8 Generating new information for substances and mixtures
1.For the purposes of determining whether a substance or a mixture entails a health or environmental hazard as set out in Annex I to this Regulation, the manufacturer, importer or downstream user may, provided that he has exhausted all other means of generating information including by applying the rules provided for in section 1 of Annex XI to Regulation (EC) No 1907/2006, perform new tests.
2.For the purposes of determining whether a substance or a mixture entails any of the physical hazards referred to in Part 2 of Annex I, the manufacturer, importer or downstream user shall perform the tests required in that Part, unless there is adequate and reliable information already available.
3.The tests referred to in paragraph 1 shall be conducted in accordance with one of the following methods:
(a)the test methods referred to in Article 13(3) of Regulation (EC) No 1907/2006;
or
(b)sound scientific principles that are internationally recognised or methods validated according to international procedures.
4.Where the manufacturer, importer or downstream user carries out new ecotoxicological or toxicological tests and analyses, these shall be carried out in compliance with Article 13(4) of Regulation (EC) No 1907/2006.
5.Where new tests for physical hazards are carried out for the purposes of this Regulation, they shall be carried out, at the latest from 1 January 2014, in compliance with a relevant recognised quality system or by laboratories complying with a relevant recognised standard.
6.Tests that are carried out for the purposes of this Regulation shall be carried out on the substance or on the mixture in the form(s) or physical state(s) in which the substance or mixture is placed on the market and in which it can reasonably be expected to be used.
CHAPTER 2 Evaluation of hazard information and decision on classification
Article 9 Evaluation of hazard information for substances and mixtures
1.Manufacturers, importers and downstream users of a substance or a mixture shall evaluate the information identified in accordance with Chapter 1 of this Title by applying to it the criteria for classification for each hazard class or differentiation in Parts 2 to 5 of Annex I, so as to ascertain the hazards associated with the substance or mixture.
2.In evaluating available test data for a substance or a mixture which have been obtained from test methods other than those referred to in Article 8(3), manufacturers, importers and downstream users shall compare the test methods employed with those indicated in that Article in order to determine whether the use of those test methods affects the evaluation referred to in paragraph 1 of this Article.
3.Where the criteria cannot be applied directly to available identified information, manufacturers, importers and downstream users shall carry out an evaluation by applying a weight of evidence determination using expert judgement in accordance with section 1.1.1 of Annex I to this Regulation, weighing all available information having a bearing on the determination of the hazards of the substance or the mixture, and in accordance with section 1.2 of Annex XI to Regulation (EC) No 1907/2006.
4.Where only the information referred to in Article 6(5) is available, manufacturers, importers and downstream users shall apply the bridging principles referred to in section 1.1.3 and in each section of Parts 3 and 4 of Annex I for the purposes of the evaluation.
However, where that information permits the application neither of the bridging principles nor the principles for using expert judgement and weight of evidence determination as described in Part 1 of Annex I, manufacturers, importers and downstream users shall evaluate the information by applying the other method or methods described in each section of Parts 3 and 4 of Annex I.
5.When evaluating the available information for the purposes of classification, the manufacturers, importers and downstream users shall consider the forms or physical states in which the substance or mixture is placed on the market and in which it can reasonably be expected to be used.
Article 10 Concentration limits and M-factors for classification of substances and mixtures
1.Specific concentration limits and generic concentration limits are limits assigned to a substance indicating a threshold at or above which the presence of that substance in another substance or in a mixture as an identified impurity, additive or individual constituent leads to the classification of the substance or mixture as hazardous.
Specific concentration limits shall be set by the manufacturer, importer or downstream user where adequate and reliable scientific information shows that the hazard of a substance is evident when the substance is present at a level below the concentrations set for any hazard class in Part 2 of Annex I or below the generic concentration limits set for any hazard class in Parts 3, 4 and 5 of Annex I.
In exceptional circumstances specific concentration limits may be set by the manufacturer, importer or downstream user where he has adequate, reliable and conclusive scientific information that a hazard of a substance classified as hazardous is not evident at a level above the concentrations set for the relevant hazard class in Part 2 of Annex I or above the generic concentration limits set for the relevant hazard class in Parts 3, 4 and 5 of that Annex.
2.M-factors for substances classified as hazardous to the aquatic environment, acute category 1 or chronic category 1, shall be established by manufacturers, importers and downstream users.
3.Notwithstanding paragraph 1, specific concentration limits shall not be set for [F33mandatoryF33] hazard classes or differentiations for substances included in [F33the GB mandatory classification and labelling listF33] .
4.Notwithstanding paragraph 2, M-factors shall not be set for [F34mandatoryF34] hazard classes or differentiations for substances included in [F34the GB mandatory classification and labelling listF34] for which an M-factor is given in that Part.
However, where an M-factor is not given in [F35the GB mandatory classification and labelling listF35] for substances classified as hazardous to the aquatic environment, acute category 1 or chronic category 1, an M-factor based on available data for the substance shall be set by the manufacturer, importer or downstream user. When a mixture including the substance is classified by the manufacturer, importer or downstream user using the summation method, this M-factor shall be used.
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6.Specific concentration limits set in accordance with paragraph 1 shall take precedence over the concentrations in the relevant sections of Part 2 of Annex I or the generic concentration limits for classification in the relevant sections of Parts 3, 4 and 5 of Annex I.
7.The Agency shall provide further guidance for the application of paragraphs 1 and 2.
Article 11 Cut-off values
1.Where a substance contains another substance, itself classified as hazardous, whether in the form of an identified impurity, additive or individual constituent, this shall be taken into account for the purposes of classification, if the concentration of the identified impurity, additive or individual constituent is equal to, or greater than, the applicable cut-off value in accordance with paragraph 3.
2.Where a mixture contains a substance classified as hazardous, whether as a component or in the form of an identified impurity or additive, this information shall be taken into account for the purposes of classification, if the concentration of that substance is equal to or greater than its cut-off value in accordance with paragraph 3.
3.The cut-off value referred to in paragraphs 1 and 2 shall be determined as set out in section 1.1.2.2 of Annex I.
Article 12 Specific cases requiring further evaluation
Where, as a result of the evaluation carried out pursuant to Article 9, the following properties or effects are identified, manufacturers, importers and downstream users shall take them into account for the purposes of classification:
adequate and reliable information demonstrates that in practice the physical hazards of a substance or a mixture differ from those shown by tests;
conclusive scientific experimental data show that the substance or mixture is not biologically available and those data have been ascertained to be adequate and reliable;
adequate and reliable scientific information demonstrates the potential occurrence of synergistic or antagonistic effects among the substances in a mixture for which the evaluation was decided on the basis of the information for the substances in the mixture.
Article 13 Decision to classify substances and mixtures
If the evaluation undertaken pursuant to Article 9 and Article 12 shows that the hazards associated with the substance or mixture meet the criteria for classification in one or more hazard classes or differentiations in Parts 2 to 5 of Annex I, manufacturers, importers and downstream users shall classify the substance or mixture in relation to the relevant hazard class or classes or differentiations by assigning the following:
one or more hazard categories for each relevant hazard class or differentiation;
subject to Article 21, one or more hazard statements corresponding to each hazard category assigned in accordance with (a).
Article 14 Specific rules for the classification of mixtures
1.The classification of a mixture shall not be affected where the evaluation of the information indicates any of the following:
(a)that the substances in the mixture react slowly with atmospheric gases, in particular oxygen, carbon dioxide, water vapour, to form different substances at low concentration;
(b)that the substances in the mixture react very slowly with other substances in the mixture to form different substances at low concentration;
(c)that the substances in the mixture may self-polymerise to form oligomers or polymers, at low concentration.
2.A mixture need not be classified for explosive, oxidising, or flammable properties as referred to in Part 2 of Annex I provided that any of the following requirements are met:
(a)none of the substances in the mixture possesses any of those properties and, on the basis of the information available to the supplier, the mixture is unlikely to present hazards of this kind;
(b)in the event of a change in the composition of a mixture, scientific evidence indicates that an evaluation of the information on the mixture will not lead to a change in classification [F37.F37]
[F38 ((c)F38] F38. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Article 15 Review of classification for substances and mixtures
1.Manufacturers, importers and downstream users shall take all reasonable steps available to them to make themselves aware of new scientific or technical information that may affect the classification of the substances or mixtures they place on the market. When a manufacturer, importer or downstream user becomes aware of such information which he considers to be adequate and reliable, that manufacturer, importer or downstream user shall without undue delay carry out a new evaluation in accordance with this Chapter.
2.Where the manufacturer, importer or downstream user introduces a change to a mixture that has been classified as hazardous, that manufacturer, importer or downstream user shall carry out a new evaluation in accordance with this Chapter where the change is either of the following:
(a)a change in the composition of the initial concentration of one or more of the hazardous constituents in concentrations at or above the limits in Table 1.2 of Part 1 of Annex I;
(b)a change in the composition involving the substitution or addition of one or more constituents in concentrations at or above the cut-off value referred to in Article 11(3).
3.A new evaluation in accordance with paragraphs 1 and 2 shall not be required if there is valid scientific justification that this will not result in a change of classification.
4.Manufacturers, importers and downstream users shall adapt the classification of the substance or the mixture in accordance with the results of the new evaluation except where there are [F39mandatoryF39] hazard classes or differentiations for substances included in [F39the GB mandatory classification and labelling listF39] .
5.For paragraphs 1 to 4 of this Article, when the substance or mixture concerned is within the scope of [F40Regulation (EC) No 1107/2009 or Regulation (EC) No 528/2012F40] , the requirements of those [F40RegulationsF40] shall also apply.
F41Article 16 Classification of substances included in the classification and labelling inventory
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TITLE III HAZARD COMMUNICATION IN THE FORM OF LABELLING
CHAPTER 1 Content of the label
Article 17 General rules
1.A substance or mixture classified as hazardous and contained in packaging shall bear a label including the following elements:
(a)the name, address and telephone number of the supplier(s);
(b)the nominal quantity of the substance or mixture in the package made available to the general public, unless this quantity is specified elsewhere on the package;
(c)product identifiers as specified in Article 18;
(d)where applicable, hazard pictograms in accordance with Article 19;
(e)where applicable, signal words in accordance with Article 20;
(f)where applicable, hazard statements in accordance with Article 21;
(g)where applicable, the appropriate precautionary statements in accordance with Article 22;
(h)where applicable, a section for supplemental information in accordance with Article 25.
2.The label shall be written in [F42EnglishF42] .
Suppliers may use more languages on their labels than [F43EnglishF43] , provided that the same details appear in all languages used.
Article 18 Product identifiers
1. The label shall include details permitting the identification of the substance or mixture (hereinafter referred to as ‘product identifiers’).
The term used for identification of the substance or mixture shall be the same as that used in the safety data sheet drawn up in accordance with Article 31 of Regulation (EC) No 1907/2006 (hereinafter referred to as ‘safety data sheet’), without prejudice to Article 17(2) of this Regulation.
2.The product identifier for a substance shall consist of at least the following:
(a)if the substance is included in [F44the GB mandatory classification and labelling listF44] , a name and an identification number as given therein;
F45(b). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(c) if the substance is not included in [F46 the GB mandatory classification and labelling list F47 ... F46] , the number provided by the CAS (hereinafter referred to as ‘the CAS number’), together with the name set out in the nomenclature provided by the IUPAC (hereinafter referred to as ‘the IUPAC Nomenclature’), or the CAS number together with another international chemical name(s); or
(d)if the CAS number is not available, the name set out in the IUPAC Nomenclature or another international chemical name(s).
Where the name in the IUPAC nomenclature exceeds 100 characters, one of the other names (usual name, trade name, abbreviation) referred to in section 2.1.2 of Annex VI to Regulation (EC) No 1907/2006 may be used provided that the notification in accordance with Article 40 includes both the name set out in the IUPAC Nomenclature and the other name used.
3.The product identifier for a mixture shall consist of both of the following:
(a)the trade name or the designation of the mixture;
(b)the identity of all substances in the mixture that contribute to the classification of the mixture as regards acute toxicity, skin corrosion or serious eye damage, germ cell mutagenicity, carcinogenicity, reproductive toxicity, respiratory or skin sensitisation, specific target organ toxicity (STOT) or aspiration hazard.
Where, in the case referred to in (b), that requirement leads to the provision of multiple chemical names, a maximum of four chemical names shall suffice, unless more than four names are needed to reflect the nature and the severity of the hazards.
The chemical names selected shall identify the substances primarily responsible for the major health hazards which have given rise to the classification and the choice of the corresponding hazard statements.
Article 19 Hazard pictograms
1.The label shall include the relevant hazard pictogram(s), intended to convey specific information on the hazard concerned.
2.Subject to Article 33, hazard pictograms shall fulfil the requirements laid down in section 1.2.1 of Annex I and in Annex V.
3.The hazard pictogram relevant for each specific classification is set out in the tables indicating the label elements required for each hazard class in Annex I.
Article 20 Signal words
1.The label shall include the relevant signal word in accordance with the classification of the hazardous substance or mixture.
2.The signal word relevant for each specific classification is set out in the tables indicating the label elements required for each hazard class in Parts 2 to 5 of Annex I.
3. Where the signal word ‘Danger’ is used on the label, the signal word ‘Warning’ shall not appear on the label.
Article 21 Hazard statements
1.The label shall include the relevant hazard statements in accordance with the classification of the hazardous substance or mixture.
2.The hazard statements relevant for each classification are set out in the tables indicating the label elements required for each hazard class in Parts 2 to 5 of Annex I.
3.F49Where a substance is included in [F48the GB mandatory classification and labelling listF48] , the hazard statement relevant for each specific classification covered by the entry ... shall be used on the label, together with the hazard statements referred to in paragraph 2 for any other classification not covered by that entry.
4.The hazard statements shall be worded in accordance with Annex III.
Article 22 Precautionary statements
1.The label shall include the relevant precautionary statements.
2.The precautionary statements shall be selected from those set out in the tables in Parts 2 to 5 of Annex I indicating the label elements for each hazard class.
3.The precautionary statements shall be selected in accordance with the criteria laid down in Part 1 of Annex IV taking into account the hazard statements and the intended or identified use or uses of the substance or the mixture.
4.The precautionary statements shall be worded in accordance with Part 2 of Annex IV.
Article 23 Derogations from labelling requirements for special cases
The specific provisions on labelling laid down in section 1.3 of Annex I shall apply in respect of the following:
transportable gas cylinders;
gas containers intended for propane, butane or liquefied petroleum gas;
aerosols and containers fitted with a sealed spray attachment and containing substances or mixtures classified as presenting an aspiration hazard;
metals in massive form, alloys, mixtures containing polymers, mixtures containing elastomers;
explosives, as referred to in section 2.1 of Annex I, placed on the market with a view to obtaining an explosive or pyrotechnic effect [F37;F37]
[F50 substances or mixtures classified as corrosive to metals but not classified as skin corrosion or as serious eye damage (Category 1).F50]
Article 24 Request for use of an alternative chemical name
1.The manufacturer, importer or downstream user of a substance in a mixture may submit a request to the Agency to use an alternative chemical name which refers to that substance in a mixture either by means of a name that identifies the most important functional chemical groups or by means of an alternative designation, where the substance meets the criteria set out in Part 1 of Annex I and where he can demonstrate that disclosure on the label or in the safety data sheet of the chemical identity of that substance puts the confidential nature of his business, in particular his intellectual property rights, at risk.
2.Any request referred to in paragraph 1 of this Article shall be made in the format [F51specified by the Agency. The Agency may require the request toF51] be accompanied by a fee.
F52...
A reduced fee shall be set for SMEs.
3.The Agency may require further information from the manufacturer, importer or downstream user making the request if such information is necessary to take a decision. If the Agency raises no objection within six weeks of the request or the receipt of further required information, the use of the requested name shall be deemed to be allowed.
[F53 4.If the Agency does not accept the request, the manufacturer, importer or downstream user may ask the Agency to review its decision.F53]
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6.Where new information shows that an alternative chemical name used does not provide sufficient information for necessary health and safety precautions to be taken at the workplace and to ensure that risks from handling the mixture can be controlled, the Agency shall review its decision on the use of that alternative chemical name. The Agency may withdraw its decision or amend it by a decision specifying which alternative chemical name is allowed to be used. If the Agency withdraws or amends its decision, the [F55manufacturer, importer or downstream user may ask the Agency to review the withdrawal or amendment.F55]
7.Where the use of an alternative chemical name has been allowed, but the classification of the substance in a mixture for which the alternative name is used no longer meets the criteria set out in section 1.4.1 of Annex I, the supplier of that substance in a mixture shall use the product identifier for the substance in accordance with Article 18 on the label and in the safety data sheet, and not the alternative chemical name.
8.For substances, whether on their own or in a mixture, where a justification in accordance with Article 10(a)(xi) of Regulation (EC) No 1907/2006 regarding information referred to in Article 119(2)(f) or (g) of that Regulation has been accepted as valid by the Agency, the manufacturer, importer or downstream user may use on the label and in the safety data sheet a name that will be made publicly available over the Internet. For those substances in a mixture for which Article 119(2)(f) or (g) of that Regulation no longer applies, the manufacturer, importer or downstream user may submit a request to the Agency to use an alternative chemical name as provided for in paragraph 1 of this Article.
9.Where the supplier of a mixture, before 1 June 2015, has demonstrated under Article 15 of Directive 1999/45/EC that the disclosure of the chemical identity of a substance in a mixture puts the confidential nature of his business at risk, he can continue to use the agreed alternative name for the purposes of this Regulation.
Article 25 Supplemental information on the label
1.Statements shall be included in the section for supplemental information on the label where a substance or mixture classified as hazardous has the physical properties or health properties referred to in sections 1.1 and 1.2 of Annex II.
The statements shall be worded in accordance with sections 1.1 and 1.2 of Annex II and Part 2 of Annex III.
Where a substance is included in [F56the GB mandatory classification and labelling listF56] , any supplemental hazard statements given therein for the substance shall be included in the supplemental information on the label.
2.A statement shall be included in the section for supplemental information on the label where a substance or mixture classified as hazardous falls within the scope of [F57Regulation (EC) No 1107/2009F57] .
The statement shall be worded in accordance with Part 4 of Annex II and Part 3 of Annex III to this Regulation.
3.The supplier may include supplemental information in the section for supplemental information on the label other than that referred to in paragraphs 1 and 2, provided that that information does not make it more difficult to identify the label elements referred to in Article 17(1) (a) to (g) and that it provides further details and does not contradict or cast doubt on the validity of the information specified by those elements.
4. Statements such as ‘non-toxic’, ‘non-harmful’, ‘non-polluting’, ‘ecological’ or any other statements indicating that the substance or mixture is not hazardous or any other statements that are inconsistent with the classification of that substance or mixture shall not appear on the label or packaging of any substance or mixture.
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6.Where a mixture contains any substance classified as hazardous, it shall be labelled in accordance with Part 2 of Annex II.
The statements shall be worded in accordance with Part 3 of Annex III and shall be placed in the supplemental information section of the label.
The label shall also include the product identifier referred to in Article 18 and the name, address and telephone number of the supplier of the mixture.
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Article 26 Principles of precedence for hazard pictograms
1.Where the classification of a substance or mixture would result in more than one hazard pictogram on the label, the following rules of precedence shall apply to reduce the number of hazard pictograms required:
(a) if the hazard pictogram ‘GHS01’ applies, the use of the hazard pictograms ‘GHS02’ and ‘GHS03’ shall be optional, except in cases where more than one of these hazard pictograms are compulsory;
(b) if the hazard pictogram ‘GHS06’ applies, the hazard pictogram ‘GHS07’ shall not appear;
(c) if the hazard pictogram ‘GHS05’ applies, the hazard pictogram ‘GHS07’ shall not appear for skin or eye irritation;
(d) if the hazard pictogram ‘GHS08’ applies for respiratory sensitisation, the hazard pictogram ‘GHS07’ shall not appear for skin sensitisation or for skin and eye irritation [F61 ; F61]
[F62 (e ) if the hazard pictogram ‘ GHS02 ’ or ‘ GHS06 ’ applies, the use of the hazard pictogram ‘ GHS04 ’ shall be optional. F62]
2.Where the classification of a substance or mixture would result in more than one hazard pictogram for the same hazard class the label shall include the hazard pictogram corresponding to the most severe hazard category for each hazard class concerned.
For substances that are included in [F63the GB mandatory classification and labelling listF63] and also subject to classification pursuant to Title II, the label shall include the hazard pictogram corresponding to the most severe hazard category for each relevant hazard class.
Article 27 Principles of precedence for hazard statements
If a substance or mixture is classified within several hazard classes or differentiations of a hazard class, all hazard statements resulting from the classification shall appear on the label, unless there is evident duplication or redundancy.
Article 28 Principles of precedence for precautionary statements
1.Where the selection of the precautionary statements results in certain precautionary statements being clearly redundant or unnecessary given the specific substance, mixture or packaging, such statements shall be omitted from the label.
2.Where the substance or mixture is supplied to the general public, one precautionary statement addressing the disposal of that substance or mixture as well as the disposal of packaging shall appear on the label, unless not required under Article 22.
In all other cases, a precautionary statement addressing disposal shall not be required, where it is clear that the disposal of the substance or mixture or the packaging does not present a hazard to human health or the environment.
3.Not more than six precautionary statements shall appear on the label, unless necessary to reflect the nature and the severity of the hazards.
Article 29 Exemptions from labelling and packaging requirements
1.F64Where the packaging of a substance or a mixture is either in such a shape or form or is so small that it is impossible to meet the requirements of Article 31 for a label ..., the label elements in accordance with the first subparagraph of Article 17(2) shall be provided in accordance with section 1.5.1 of Annex I.
2.If the full label information cannot be provided in the way specified in paragraph 1 the label information may be reduced in accordance with section 1.5.2 of Annex I.
3.When a hazardous substance or mixture referred to in Part 5 of Annex II is supplied to the general public without packaging it shall be accompanied by a copy of the label elements in accordance with Article 17.
4.For certain mixtures classified as hazardous to the environment, exemptions to certain provisions on environmental labelling or specific provisions in relation to environmental labelling may be determined in accordance with the procedure referred to in Article 53, where it can be demonstrated that there would be a reduction in the environmental impact. Such exemptions or specific provisions are defined in Part 2 of Annex II.
F654a .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
5.The [F66Secretary of State or a Devolved AuthorityF66] may request the Agency to prepare and submit to it further draft exemptions from labelling and packaging requirements.
Article 30 Updating information on labels
1.The supplier shall ensure that the label is updated, without undue delay, following any change to the classification and labelling of that substance or mixture, where the new hazard is more severe or where new supplemental labelling elements are required under Article 25, taking into account the nature of the change as regards the protection of human health and the environment. Suppliers shall cooperate in accordance with Article 4(9) to complete the changes to the labelling without undue delay.
2.Where labelling changes are required other than those referred to in paragraph 1, the supplier shall ensure that the label is updated within 18 months.
3.The supplier of a substance or a mixture within the scope of [F67Regulation (EC) No 1107/2009 or Regulation (EC) No 528/2012F67] shall update the label in accordance with those [F68RegulationsF68] .
CHAPTER 2 Application of labels
Article 31 General rules for the application of labels
1.Labels shall be firmly affixed to one or more surfaces of the packaging immediately containing the substance or mixture and shall be readable horizontally when the package is set down normally.
2.The colour and presentation of any label shall be such that the hazard pictogram stands out clearly.
3.The label elements referred to in Article 17(1) shall be clearly and indelibly marked. They shall stand out clearly from the background and be of such size and spacing as to be easily read.
4.The shape, colour and the size of a hazard pictogram as well as the dimensions of the label shall be as set out in section 1.2.1 of Annex I.
5.A label shall not be required when the label elements referred to in Article 17(1) are shown clearly on the packaging itself. In such cases, the requirements of this Chapter applicable to a label shall be applied to the information shown on the packaging.
Article 32 Location of information on the label
1.The hazard pictograms, signal word, hazard statements and precautionary statements shall be located together on the label.
2.The supplier may decide the order of the hazard statements on the label. However, subject to paragraph 4, all hazard statements shall be grouped on the label by language [F69, where languages other than English are usedF69] .
The supplier may decide the order of the precautionary statements on the label. However, subject to paragraph 4, all precautionary statements shall be grouped on the label by language [F69, where languages other than English are usedF69] .
3.Groups of hazard statements and groups of precautionary statements referred to in paragraph 2 shall be located together on the label by language [F70, where languages other than English are usedF70] .
4.The supplemental information shall be placed in the supplemental information section referred to in Article 25, and shall be located with the other label elements specified in Article 17(1)(a) to (g).
5.In addition to its use in hazard pictograms, colour may be used on other areas of the label to implement special labelling requirements.
6.Label elements resulting from the requirements provided for in other [[F71,F72 assimilatedF72] lawF71] shall be placed in the section for supplemental information on the label referred to in Article 25.
Article 33 Specific rules for labelling of outer packaging, inner packaging and single packaging
1.Where a package consists of an outer and an inner packaging, together with any intermediate packaging, and the outer packaging meets labelling provisions in accordance with the rules on the transport of dangerous goods, the inner and any intermediate packaging shall be labelled in accordance with this Regulation. The outer packaging may also be labelled in accordance with this Regulation. Where the hazard pictogram(s) required by this Regulation relate to the same hazard as in the rules for the transport of dangerous goods, the hazard pictogram(s) required by this Regulation need not appear on the outer packaging.
2.Where the outer packaging of a package is not required to meet labelling provisions in accordance with rules on the transport of dangerous goods, both the outer and any inner packaging, including any intermediate packaging, shall be labelled in accordance with this Regulation. However, if the outer packaging permits the inner or intermediate packaging labelling to be clearly seen, the outer packaging need not be labelled.
3.Single packages that meet the labelling provisions in accordance with the rules on the transport of dangerous goods shall be labelled both in accordance with this Regulation and the rules on the transport of dangerous goods. Where the hazard pictogram(s) required by this Regulation relate to the same hazard as in rules on the transport of dangerous goods, the hazard pictogram(s) required by this Regulation need not appear.
F73Article 34 Report on communication on safe use of chemicals
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TITLE IV PACKAGING
Article 35 Packaging
1.Packaging containing hazardous substances or mixtures shall satisfy the following requirements:
(a)the packaging shall be designed and constructed so that its contents cannot escape, except in cases where other more specific safety devices are prescribed;
(b)the materials constituting the packaging and fastenings shall not be susceptible to damage by the contents, or liable to form hazardous compounds with the contents;
(c)the packaging and fastenings shall be strong and solid throughout to ensure that they will not loosen and will safely meet the normal stresses and strains of handling;
(d)packaging fitted with replaceable fastening devices shall be designed so that it can be refastened repeatedly without the contents escaping.
2.Packaging containing a hazardous substance or a mixture supplied to the general public shall not have either a shape or design likely to attract or arouse the active curiosity of children or to mislead consumers, or have a similar presentation or a design used for foodstuff or animal feeding stuff or medicinal or cosmetic products, which would mislead consumers.
Where the packaging contains a substance or mixture which meets the requirements in section 3.1.1 of Annex II it shall have a child-resistant fastening in accordance with sections 3.1.2, 3.1.3 and 3.1.4.2 of Annex II.
Where the packaging contains a substance or mixture which meets the requirements in section 3.2.1 of Annex II it shall bear a tactile warning of danger in accordance with section 3.2.2 of Annex II.
[F74 Where a liquid consumer laundry detergent, as defined in Article 2(1a) of Regulation (EC) No 648/2004 of the European Parliament and of the Council(1), is contained in a soluble packaging for single use, the additional requirements of section 3.3 of Annex II shall apply.F74]
3.The packaging of substances and mixtures shall be deemed to satisfy the requirements of paragraph 1(a), (b) and (c) if it complies with the requirements of the rules on the transport of dangerous goods by air, sea, road, rail or inland waterways.
TITLE V [F75MANDATORY CLASSIFICATION AND LABELLING OF SUBSTANCES F76...F75]
CHAPTER 1 [F77Establishing mandatory classification of substancesF77]
Article 36 [F78MandatoryF78] classification and labelling of substances
1.F80A substance that fulfils the criteria set out in Annex I for the following shall normally be subject to [F79mandatoryF79] classification and labelling in accordance with Article 37 ...:
(a)respiratory sensitisation, category 1 (Annex I, section 3.4);
(b)germ cell mutagenicity, category 1A, 1B or 2 (Annex I, section 3.5);
(c)carcinogenicity, category 1A, 1B or 2 (Annex I, section 3.6);
(d)reproductive toxicity, category 1A, 1B or 2 (Annex I, section 3.7).
2.F83,F84A substance that is an active substance in the meaning of [F81Regulation (EC) No 1107/2009 or Regulation (EC) No 528/2012F81] shall normally be subject to [F82mandatoryF82] classification and labelling. For such substances, the procedures set out in Article 37 ..., ... shall apply.
3.F87,F89Where a substance fulfils the criteria for other hazard classes or differentiations than those referred to in paragraph 1 and does not fall under paragraph 2, a [F85mandatoryF85] classification and labelling [F86requirementF86] in accordance with Article 37 ... may also be added to [F88the GB mandatory classification and labelling listF88] on a case-by-case basis, if justification is provided demonstrating the need for such action ....
[F90Article 37 Procedure for mandatory classification and labelling
1.This Article applies in relation to a substance which is the subject of a proposal for a new or revised classification and labelling requirement and, where appropriate, specific concentration limits or M-factors.
2.In this Article—
“ fast-track proposal ” means a proposal from a territory (including the European Union) or state authority which in the opinion of the Agency—
(a)has adopted the GHS in a similar way to the United Kingdom; and
(b)has a transparent classification proposal system based on public consultation;
“ GHS ” means the United Nations Globally Harmonised System of Classification and Labelling of Chemicals, as revised from time to time;
“ proposal ” means a proposal referred to in paragraph 1;
“ state authority ” means an authority or organisation which acts for a territory;
“ work plan ” means the plan published and maintained by the Agency in accordance with paragraph 3.
3.The Agency must publish, keep under review and in the event of change publish an updated version of a work plan for its evaluation of proposals, and must identify any fast-track proposals for inclusion in the work plan, having particular regard to the provisions of Article 36. The Agency must consult the Devolved Authorities when—
(a)producing;
(b)reviewing;
(c)making any material changes to,
4.Paragraph 5 of this Article applies to fast-track proposals, and paragraphs 6 to 9 apply to other proposals.
5.In respect of each fast-track proposal—
(a)the Agency must publish a technical report on the proposal in accordance with the Agency’s work plan;
(b)where the Agency considers that it is appropriate to recommend that a new or revised mandatory classification and labelling requirement is imposed, the Agency must within 12 months of the publication by the Agency of the technical report submit a recommendation to the Secretary of State concerning the proposal;
(c)within 3 months of the recommendation being submitted by the Agency, the Secretary of State must—
(i)decide whether to accept the recommendation;
(ii)publish that decision, together with reasons for the decision;
(iii)where the decision referred to in paragraph (i) is to accept the recommendation, specify (alongside the decision and the reasons for the decision) the date from when any new or revised classification and labelling requirement must be complied with;
(iv)notify the Agency of the decision and details referred to in paragraphs (ii) and (iii);
(d)the Secretary of State’s functions under subparagraph (c)(i) and (iii) are subject to the consent requirement in Article 53B;
(e)within 1 month of the Secretary of State notifying the Agency of a decision in accordance with subparagraph (c)(iv), the Agency must update the GB mandatory classification and labelling list accordingly, making clear the date from when any new or revised classification and labelling requirement must be complied with.
6.Proposals referred to in this paragraph are not fast-track proposals, and a proposal under subparagraph (a) or (b) must comply with the requirements specified in paragraph 8—
(a)a proposal may be produced by the Agency or submitted to the Agency by a competent authority;
(b)subject to paragraph 7, a manufacturer, importer or downstream user of a substance may submit a proposal in relation to a substance to the Agency where there is no entry in the GB mandatory classification and labelling list for such substance in relation to the hazard class or differentiation covered by that proposal;
(c)subject to paragraph 7, a manufacturer, importer or downstream user of a substance who has new information which may lead to a change of the mandatory classification and labelling elements of a substance in the GB mandatory classification and labelling list must submit a proposal to the Agency for a revised classification.
7.Paragraph 6(b) and (c) does not apply to manufacturers, importers or downstream users of substances established in Northern Ireland who supply qualifying Northern Ireland goods directly to Great Britain.
8.A proposal—
(a)under paragraph 6(a) or (b) must follow the format set out in Part 2 of Annex VI and must contain the relevant information provided for in Part 1 of Annex VI;
(b)under paragraph 6(b) which concerns the mandatory classification and labelling of a substance in accordance with Article 36(3) must additionally be accompanied by the relevant fee as determined by the Agency.
9.For each proposal which is not a fast-track proposal—
(a)within 12 months of the proposal being received or produced by the Agency, during which time the parties concerned must be given an opportunity to comment, the Agency must publish a technical report on the proposal;
(b)within 6 months of publishing the technical report (which may in exceptional circumstances be extended to 12 months), the Agency must publish an opinion on the proposal;
(c)where the Agency considers that it is appropriate to recommend that a new or revised mandatory classification and labelling requirement is imposed, the Agency must within 12 months of the opinion being published submit a recommendation to the Secretary of State to give effect to the opinion;
(d)within 3 months of the recommendation being submitted by the Agency, the Secretary of State must—
(i)decide whether to accept the recommendation;
(ii)publish that decision, together with reasons for the decision;
(iii)where the decision is to accept the recommendation, specify (alongside the decision and the reasons for the decision) the date from when any new or revised classification and labelling requirement must be complied with;
(iv)notify the Agency of the decision and details referred to in paragraphs (ii) and (iii);
(e)the Secretary of State’s functions under subparagraph (d)(i) and (iii) are subject to the consent requirement in Article 53B;
(f)within one month of the Secretary of State notifying the Agency of a decision in accordance with subparagraph (d)(iv), the Agency must update the GB mandatory classification and labelling list accordingly, making clear the date from when any new or revised classification and labelling requirement must be complied with.F90]
F90Article 37A Procedure for mandatory classification and labelling of substances where Article 37(1) does not apply
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Article 38 Content of opinions and decisions for [F91mandatoryF91] classification and labelling in [F91the GB mandatory classification and labelling listF91] ; accessibility of information
F92A1.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.Any opinion [F93of the Agency referred to in [F94 Article 37 must specify the reasons for the opinion, andF94,F93]] shall at least specify for each substance:
(a)the identity of the substance as specified in sections 2.1 to 2.3.4 of Annex VI to Regulation (EC) No 1907/2006;
(b)the classification of the substance referred to in Article 36, including a statement of reasons;
(c)the specific concentration limits or M-factors, where applicable;
(d)the label elements specified in points (d), (e) and (f) of Article 17(1) for the substance, together with any supplemental hazard statements for the substance, determined in accordance with Article 25(1);
(e)any other parameter enabling an assessment to be made of the health or environmental hazard of mixtures containing the hazardous substance in question or of substances containing such hazardous substances as identified impurities, additives and constituents, if relevant.
[F95 2.When making publicly available an opinion or a decision as referred to in Article 37 F96..., the Agency must not publish any information in relation to which paragraph 3 applies.F95]
[F97 3.This paragraph applies to information which has been made available to the Agency in relation to which a person has submitted a justification, accepted by the Agency as valid, as to why publication of the information is potentially harmful to the commercial interests of that person or any other person.F97]
[F98Article 38A GB mandatory classification and labelling list
The Agency must establish, maintain and publish electronically a list (to be called “the GB mandatory classification and labelling list”) of all the mandatory classifications and accompanying labelling requirements made by the Secretary of State in accordance with Article 37 F99 .... F98]
F100CHAPTER 2 [F101GB notification databaseF101]
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TITLE VI [F103HELPDESK AND APPOINTMENT OF BODIESF103]
F104Article 43 Appointment of competent authorities and enforcement authorities and cooperation between authorities
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Article 44 Helpdesk
[F105 The Agency must establish a helpdeskF105] to provide advice to manufacturers, importers, distributors, downstream users and any other interested parties on their respective responsibilities and obligations under this Regulation.
Article 45 Appointment of bodies responsible for receiving information relating to emergency health response
1.[F106 The Secretary of State in relation to England, and the Devolved Authorities in relation to their respective countriesF106] shall appoint a body or bodies responsible for receiving information relevant, in particular, for formulating preventative and curative measures, in particular in the event of emergency health response, from importers and downstream users placing mixtures on the market. This information shall include the chemical composition of mixtures placed on the market and classified as hazardous on the basis of their health or physical effects, including the chemical identity of substances in mixtures for which a request for use of an alternative chemical name has been accepted by the Agency, in accordance with Article 24.
[F107 1A.The Secretary of State may carry out the function set out in paragraph 1 in relation to Scotland or Wales, if the Devolved Authority in question has consented to the Secretary of State exercising that function.F107]
2.The appointed bodies shall provide all requisite guarantees for maintaining the confidentiality of the information received. Such information may only be used:
(a)to meet medical demand by formulating preventative and curative measures, in particular in the event of an emergency;
and
(b)where requested by the [F108Secretary of State or the relevant Devolved AuthorityF108] , to undertake statistical analysis to identify where improved risk management measures may be needed.
The information shall not be used for other purposes.
[F109 3.The appointed bodies shall have at their disposal any information that is voluntarily provided by importers and downstream users placing mixtures on the market, or that is required to be provided in accordance with regulations made under Article 45(4), to carry out the tasks for which the appointed bodies are responsible.F109]
[F110 4 .The Secretary of State may by regulations specify the information relating to emergency health response and preventative measures required for the purposes of this Article, following consultation with relevant stakeholders as referred to in paragraph 5.
5.Before making regulations, the Secretary of State must consult—
(a)the body or bodies appointed under paragraph 1,
and
(b)any person or body who the Secretary of State considers is representative of importers, if any,
(c)any person or body who the Secretary of State considers is representative of downstream users, if any, and
(d)any other person who the Secretary of State considers appropriate.
6.The Secretary of State’s regulation-making function under paragraph 4 is subject to the consent requirement in Article 53B.F110]
F111Article 46 Enforcement and reporting
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F112Article 47 Penalties for non-compliance
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TITLE VII COMMON AND FINAL PROVISIONS
Article 48 Advertisement
1.Any advertisement for a substance classified as hazardous shall mention the hazard classes or hazard categories concerned.
2.Any advertisement for a mixture classified as hazardous or covered by Article 25(6) which allows a member of the general public to conclude a contract for purchase without first having sight of the label shall mention the type or types of hazard indicated on the label.
The first subparagraph shall be without prejudice to [F113the Consumer Contracts (Information, Cancellation and Additional Charges) Regulations 2013F113] on the protection of consumers in respect of distance contracts.
Article 49 Obligation to maintain information and requests for information
1.The supplier shall assemble and keep available all the information used by that supplier for the purposes of classification and labelling under this Regulation for a period of at least 10 years after the substance or the mixture was last supplied by that supplier.
The supplier shall keep this information together with the information required in Article 36 of Regulation (EC) No 1907/2006.
2.In the event of a supplier ceasing activity, or transferring part or all of his operations to a third party, the party responsible for liquidating the supplier's undertaking or assuming responsibility for the placing on the market of the substance or mixture concerned shall be bound by the obligation in paragraph 1 in place of the supplier.
3.The [F114competent authorities, enforcing authoritiesF114] or the Agency may require the supplier to submit to it any information referred to in the first subparagraph of paragraph 1.
However, where that information is available to the Agency as part of a registration pursuant to Regulation (EC) No 1907/2006 or a notification pursuant to Article 40 of this Regulation, the Agency shall use that information and the authority [F115in questionF115] shall address itself to the Agency.
[F116 4. For the purposes of this Article, “enforcing authorities” has the meaning given by regulation 18 of the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013 . F116]
Article 50 Tasks of the Agency
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2.F118The ... Agency shall:
(a)provide industry with technical and scientific guidance and tools where appropriate on how to comply with the obligations laid down by this Regulation;
(b)F120provide competent authorities with technical and scientific guidance on the operation of this Regulation and provide support to the [F119helpdeskF119] established ... under Article 44.
F121Article 51 Free movement clause
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[F122Article 52 Safeguard clause
1.The Secretary of State or a Devolved Authority may take appropriate provisional measures in respect of a substance or mixture if they—
(a)have justifiable grounds for believing that the substance or mixture, although satisfying the requirements of this Regulation, constitutes a serious risk to human health or the environment due to reasons of classification, labelling or packaging; and
(b)have competence to take the provisional measures, within the meaning of paragraphs 6 to 8.
2.A provisional measure taken by a Devolved Authority applies only in relation to the territory in relation to which it has competence.
3.Where the Secretary of State takes a provisional measure, the Secretary of State must immediately inform the Devolved Authorities, giving the reasons for the decision. Where a Devolved Authority takes a provisional measure, it must immediately inform the other Devolved Authorities and the Secretary of State, giving the reasons for the decision.
4.Within 90 days of a provisional measure being taken—
(a)in the case of a provisional measure relating to classification or labelling of a substance—
(i)where the Secretary of State took the measure, the Secretary of State must request the Agency to produce a proposal for a new or revised mandatory classification and labelling requirement under Article 37A(2),
(ii)where a Devolved Authority took the measure, the Competent Authority for that country must request the Agency to produce a proposal for a new or revised mandatory classification and labelling requirement under Article 37A(2);
(b)in the case of a provisional measure that falls within the scope of Article 53—
(i)where the Secretary of State took the measure, the Secretary of State must decide whether or not to make the measure permanent by making regulations under Article 53,
(ii)where a Devolved Authority took the measure, it must decide whether or not to request the Secretary of State to make the measure permanent by making regulations under Article 53.
5.The taker of the provisional measure must revoke that measure, when—
(a)in the case of a provisional measure relating to the classification or labelling of a substance, the Secretary of State makes a decision under Article 37A;
(b)in the case of a provisional measure that falls within the scope of Article 53—
(i)where paragraph 4(b)(i) of this Article applies, the Secretary of State either decides not to make the measure permanent or makes regulations under Article 53 to make the measure permanent, or
(ii)where paragraph 4(b)(ii) of this Article applies, the Devolved Authority decides not to request the Secretary of State to make the measure permanent.
6.The Secretary of State has competence to take a provisional measure if, or to the extent that, the exercise of the function to take that measure—
(a)relates to England;
(b)relates to Scotland and is not within devolved competence (within the meaning of section 54 of the Scotland Act 1998);
(c)relates to Wales and is not within devolved competence (within the meaning of section 58A(7) and (8) of the Government of Wales Act 2006).
7.The Scottish Ministers have competence to take a provisional measure if, or to the extent that, the exercise of the function to take that measure is within devolved competence (within the meaning of section 54 of the Scotland Act 1998).
8.The Welsh Ministers have competence to take a provisional measure if, or to the extent that, the exercise of the function to take that measure is within devolved competence (within the meaning of section 58A(7) and (8) of the Government of Wales Act 2006).F122]
Article 53 Adaptations to technical and scientific progress
[F123 1 .[F124 The Secretary of State may by regulations amendF124] Article 6(5), Article 11(3), Articles 12 and 14, point (b) of Article 18(3), Article 23, Articles 25 to 29, the second and third subparagraphs of Article 35(2) and Annexes I to VIII in order to adapt them to technical and scientific progress, taking due account of the further development of the GHS, in particular any UN amendments relating to the use of information on similar mixtures, and considering the developments in internationally recognised chemical programmes and of the data from accident databases.
F125...F123]
F1262.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
[F127Article 53A Regulation making power
1.Any power to make regulations conferred on the Secretary of State by this Regulation is exercisable by statutory instrument.
2.Such regulations may—
(a)contain incidental, supplemental, consequential and transitional provision; and
(b)may make different provision for different purposes.
3.A statutory instrument containing regulations made under this Regulation is subject to annulment in pursuance of a resolution of either House of Parliament.
4.The function of making regulations under this Regulation is subject to the consent requirement in Article 53B.F127]
[F127Article 53B The consent requirement
1.Where any provision of this Regulation states that a function is subject to the consent requirement in this Article, the function may be exercised in a particular instance only if the person exercising it has obtained the consent or consents (if any) required by paragraphs 2 to 4.
2.The consent of the Scottish Ministers is required if, or to the extent that, the exercise of the function is within devolved competence (within the meaning of section 54 of the Scotland Act 1998) whether or not the exercise of the function also relates to a part of the United Kingdom other than Scotland.
3.The consent of the Welsh Ministers is required if, or to the extent that, the exercise of the function is within devolved competence (within the meaning of section 58A(7) and (8) of the Government of Wales Act 2006) whether or not the exercise of the function also relates to a part of the United Kingdom other than Wales.F127]
F128 Article 53a Exercise of the delegation
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F129 Article 53b Urgency procedure
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F130 Article 53c Separate delegated acts for different delegated powers
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F131Article 54 Committee procedure
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Article 55 Amendments to Directive 67/548/EEC
Directive 67/548/EEC shall be amended as follows:
in Article 1(2), the second subparagraph shall be deleted;
Article 4 shall be amended as follows:
paragraph 3 shall be replaced by the following:
‘3.Where an entry containing the harmonised classification and labelling for a particular substance has been included in Part 3 of Annex VI to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures(2), the substance shall be classified in accordance with that entry and paragraphs 1 and 2 shall not apply to the danger categories covered by that entry.’;
paragraph 4 shall be deleted;
Article 5 shall be amended as follows:
paragraph 1, second subparagraph shall be deleted;
paragraph 2 shall be replaced by the following:
‘2.The measures in the first subparagraph of paragraph 1 shall apply until the substance is listed in Part 3 of Annex VI to Regulation (EC) No 1272/2008 for the danger categories covered by that entry or until a decision not to list it has been taken in accordance with the procedure laid down in Article 37 of Regulation (EC) No 1272/2008.’;
Article 6 shall be replaced by the following:
‘Article 6 Obligation to carry out investigations
Manufacturers, distributors and importers of substances which appear in the EINECS but for which no entry has been included in Part 3 of Annex VI to Regulation (EC) No 1272/2008 shall carry out an investigation to make themselves aware of the relevant and accessible data which exist concerning the properties of such substances. On the basis of this information, they shall package and provisionally label dangerous substances according to the rules laid down in Articles 22 to 25 of this Directive and the criteria in Annex VI to this Directive.’;
Article 22(3) and (4) shall be deleted;
Article 23(2) shall be amended as follows:
in point (a), the words ‘Annex I’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’;
in point (c), the words ‘Annex I’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’;
in point (d), the words ‘Annex I’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’;
in point (e), the words ‘Annex I’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’;
in point (f), the words ‘Annex I’ shall be replaced by ‘Part 3 of Annex VI of Regulation (EC) No 1272/2008’;
Article 24(4) second subparagraph shall be deleted;
Article 28 shall be deleted;
Article 31(2) and (3) shall be deleted;
the following Article shall be inserted after Article 32:
‘Article 32a Transitional provision regarding labelling and packaging of substances
Articles 22 to 25 shall not apply to substances from 1 December 2010.’;
Annex I shall be deleted.
Article 56 Amendments to Directive 1999/45/EC
Directive 1999/45/EC shall be amended as follows:
in Article 3(2), first indent, the words ‘Annex I to Directive 67/548/EEC’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures(3).
the words ‘Annex I to Directive 67/548/EEC’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’ in:
Article 3(3);
Article 10(2), points 2.3.1, 2.3.2, 2.3.3 and 2.4 first indent;
Annex II, points (a) and (b) and the last paragraph of the Introduction;
Annex II, Part A,
point 1.1.1 (a) and (b),
point 1.2 (a) and (b),
point 2.1.1 (a) and (b),
point 2.2 (a) and (b),
point 2.3 (a) and (b),
point 3.1.1 (a) and (b),
point 3.3 (a) and (b),
point 3.4 (a) and (b),
point 4.1.1 (a) and (b),
point 4.2.1 (a) and (b),
point 5.1.1 (a) and (b),
point 5.2.1 (a) and (b),
point 5.3.1 (a) and (b),
point 5.4.1 (a) and (b),
point 6.1 (a) and (b),
point 6.2 (a) and (b),
point 7.1 (a) and (b),
point 7.2 (a) and (b),
point 8.1 (a) and (b),
point 8.2 (a) and (b),
point 9.1 (a) and (b),
point 9.2 (a) and (b),
point 9.3 (a) and (b),
point 9.4 (a) and (b);
Annex II, the introductory paragraph of Part B;
Annex III, point (a) and (b) of the Introduction;
Annex III, Part A, section (a) Aquatic environment
point 1.1 (a) and (b),
point 2.1 (a) and (b),
point 3.1 (a) and (b),
point 4.1 (a) and (b),
point 5.1 (a) and (b),
point 6.1 (a) and (b),
Annex III, Part A, section (b) Non-aquatic environment point 1.1 (a) and (b);
Annex V, section A points 3 and 4;
Annex V, section B point 9;
Annex VI, Part A, the third column of the table under point 2;
Annex VI Part B point 1, first paragraph, and the first column of the table under point 3;
Annex VIII, Appendix 1, second column of the table;
Annex VIII, Appendix 2, second column of the table;
in Annex VI, Part B, point 1, paragraph 3 first indent and paragraph 5, the words ‘Annex I’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’;
in Annex VI, Part B, point 4.2, final paragraph, the words ‘Annex I to Directive 67/548/EEC (19th adaptation)’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’.
Article 57 Amendments to Regulation (EC) No 1907/2006 from the entry into force of this Regulation
Regulation (EC) No 1907/2006 shall be amended as from the entry into force of this Regulation as follows:
Article 14(2) shall be amended as follows:
point (b) shall be replaced by the following:
the specific concentration limits that have been set in Part 3 of Annex VI to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures(4);
for substances classified as hazardous to the aquatic environment, if a multiplying factor (hereinafter referred to as “M-factor”) has been set in Part 3 of Annex VI to Regulation (EC) No 1272/2008, the cut-off value in Table 1.1 of Annex I to that Regulation adjusted using the calculation set out in section 4.1 of Annex I to that Regulation;’;
point (e) shall be replaced by the following:
the specific concentration limits given in an agreed entry in the classification and labelling inventory referred to in Article 42 of Regulation (EC) No 1272/2008;
for substances classified as hazardous to the aquatic environment, if an M-factor has been set in an agreed entry in the classification and labelling inventory referred to in Article 42 of Regulation (EC) No 1272/2008, the cut-off value in Table 1.1 of Annex I to that Regulation adjusted using the calculation set out in section 4.1 of Annex I to that Regulation;’;
Article 31 shall be amended as follows:
paragraph 8 shall be replaced by the following:
‘8.A safety data sheet shall be provided free of charge on paper or electronically no later than the date on which the substance or mixture is first supplied.’;
the following paragraph shall be added:
‘10.Where substances are classified in accordance with Regulation (EC) No 1272/2008 during the period from its entry into force until 1 December 2010, that classification may be added in the safety data sheet together with the classification in accordance with Directive 67/548/EEC.
From 1 December 2010 until 1 June 2015, the safety data sheets for substances shall contain the classification according to both Directive 67/548/EEC and Regulation (EC) No 1272/2008.
Where mixtures are classified in accordance with Regulation (EC) No 1272/2008 during the period from its entry into force until 1 June 2015, that classification may be added in the safety data sheet, together with the classification in accordance with Directive 1999/45/EC. However, until 1 June 2015, where substances or mixtures are both classified and labelled in accordance with Regulation (EC) No 1272/2008 that classification shall be provided in the safety data sheet, together with the classification in accordance with Directives 67/548/EEC and 1999/45/EC respectively, for the substance, the mixture and its constituents.’;
Article 56(6)(b) shall be replaced by the following:
for all other substances, below the lowest of the concentration limits specified in Directive 1999/45/EC or in Part 3 of Annex VI to Regulation (EC) No 1272/2008 which result in the classification of the mixture as dangerous.’;
Article 59(2) and 3 shall be amended as follows:
in paragraph 2, the second sentence shall be replaced by the following:
‘The dossier may be limited, if appropriate, to a reference to an entry in Part 3 of Annex VI to Regulation (EC) No 1272/2008.’;
in paragraph 3, the second sentence shall be replaced by the following:
‘The dossier may be limited, if appropriate, to a reference to an entry in Part 3 of Annex VI to Regulation (EC) No 1272/2008.’;
in Article 76(1)(c), the words ‘Title XI’ shall be replaced by ‘Title V of Regulation (EC) No 1272/2008’;
Article 77 shall be amended as follows:
in paragraph 2, the first sentence of point (e) shall be replaced by the following:
establishing and maintaining database(s) with information on all registered substances, the classification and labelling inventory and the harmonised classification and labelling list established in accordance with Regulation (EC) No 1272/2008;’;
in paragraph 3, point (a), the words ‘Titles VI to XI’ shall be replaced by ‘Titles VI to X’;
Title XI shall be deleted;
Annex XV, sections I and II shall be amended as follows:
section I shall be amended as follows:
the first indent shall be deleted;
the second indent shall be replaced by the following:
‘the identification of CMRs, PBTs, vPvBs, or a substance of equivalent concern in accordance with Article 59,’;
in section II, point 1 shall be deleted;
the table in Annex XVII shall be amended as follows:
the column ‘Designation of the substance, of the groups of substances or of the preparation’, shall be amended as follows:
entries 28, 29 and 30 shall be replaced by the following:
‘28. Substances which appear in Part 3 of Annex VI to Regulation (EC) No 1272/2008 classified as carcinogen category 1A or 1B (Table 3.1) or carcinogen category 1 or 2 (Table 3.2) and listed as follows:
Carcinogen category 1A (Table 3.1)/carcinogen category 1 (Table 3.2) listed in Appendix 1
Carcinogen category 1B (Table 3.1)/carcinogen category 2 (Table 3.2) listed in Appendix 2
29. Substances which appear in Part 3 of Annex VI to Regulation (EC) No 1272/2008 classified as germ cell mutagen category 1A or 1B (Table 3.1) or mutagen category 1 or 2 (Table 3.2) and listed as follows:
Mutagen category 1A (Table 3.1)/mutagen category 1 (Table 3.2) listed in Appendix 3
Mutagen category 1B (Table 3.1)/mutagen category 2 (Table 3.2) listed in Appendix 4
30. Substances which appear in Part 3 of Annex VI to Regulation (EC) No 1272/2008 classified as toxic to reproduction category 1A or 1B (Table 3.1) or toxic to reproduction category 1 or 2 (Table 3.2) and listed as follows:
Reproductive toxicant category 1A adverse effects on sexual function and fertility or on development (Table 3.1) or reproductive toxicant category 1 with R60 (May impair fertility) or R61 (May cause harm to the unborn child) (Table 3.2) listed in Appendix 5
Reproductive toxicant category 1B adverse effects on sexual function and fertility or on development (Table 3.1) or reproductive toxicant category 2 with R60 (May impair fertility) or R61 (May cause harm to the unborn child) (Table 3.2) listed in Appendix 6’;
in the column ‘Conditions of restriction’, in entry 28, the first indent of point 1 shall be replaced by the following:
‘either the relevant specific concentration limit specified in Part 3 of Annex VI to Regulation (EC) No 1272/2008, or’;
Appendices 1 to 6 to Annex XVII shall be amended as follows:
the Foreword shall be amended as follows:
in the section entitled ‘Substances’, the words ‘Annex I to Directive 67/548/EEC’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’;
in the section entitled ‘Index number’, the words ‘Annex I to Directive 67/548/EEC’ shall be replaced by ‘Part 3 of Annex VI to Regulation (EC) No 1272/2008’;
in the section entitled ‘Notes’, the words ‘the foreword of Annex I to Directive 67/548/EEC’ shall be replaced by ‘Part 1 of Annex VI to Regulation (EC) No 1272/2008’;
Note A shall be replaced by the following:
‘Note A:
Without prejudice to Article 17(2) of Regulation (EC) No 1272/2008, the name of the substance must appear on the label in the form of one of the designations given in Part 3 of Annex VI to that Regulation.
In that Part, use is sometimes made of a general description such as “... compounds” or “... salts”. In this case, the supplier who places such a substance on the market is required to state on the label the correct name, due account being taken of Section 1.1.1.4 of Annex VI to Regulation (EC) No 1272/2008.
In accordance with Regulation (EC) No 1272/2008, where a substance is included in Part 3 of Annex VI to that Regulation, the labelling elements relevant for each specific classification covered by the entry in that Part shall be included in the label, together with the applicable label elements for any other classification not covered by that entry, and any other applicable label elements in accordance with Article 17 of that Regulation.
For substances belonging to one particular group of substances included in Part 3 of Annex VI to Regulation (EC) No 1272/2008, the labelling elements relevant for each specific classification covered by the entry in that Part shall be included in the label, together with the applicable label elements for any other classification not covered by that entry, and any other applicable label elements in accordance with Article 17 of that Regulation.
For substances belonging to more than one group of substances included in Part 3 of Annex VI to Regulation (EC) No 1272/2008, the labelling elements relevant for each specific classification covered by both entries in that Part shall be included in the label, together with the applicable label elements for any other classification not covered by that entry, and any other applicable label elements in accordance with Article 17 of that Regulation. In cases where two different classifications are given in the two entries for the same hazard class or differentiation, the classification reflecting the more severe classification shall be used.’;
Note D shall be replaced by the following:
‘Note D:
Certain substances which are susceptible to spontaneous polymerisation or decomposition are generally placed on the market in a stabilised form. It is in this form that they are listed in Part 3 of Annex VI to Regulation (EC) No 1272/2008.
However, such substances are sometimes placed on the market in a non-stabilised form. In this case, the supplier who places such a substance on the market must state on the label the name of the substance followed by the words “non-stabilised”.’;
Note E shall be deleted;
Note H shall be replaced by the following:
‘Note H:
The classification and label shown for this substance applies to the hazard or hazards indicated by the hazard statement or hazard statements in combination with the hazard classification shown. The requirements of Article 4 of Regulation (EC) No 1272/2008 on suppliers of this substance apply to all other hazard classes, differentiations and categories.
The final label shall follow the requirements of section 1.2 of Annex I to Regulation (EC) No 1272/2008.’;
Note K shall be replaced by the following:
‘Note K:
The classification as a carcinogen or mutagen need not apply if it can be shown that the substance contains less than 0,1 % w/w 1,3-butadiene (Einecs No 203-450-8). If the substance is not classified as a carcinogen or mutagen, at least the precautionary statements (P102-)P210-P403 should apply. This note applies only to certain complex oil-derived substances in Part 3 of Annex VI to Regulation (EC) No 1272/2008.’;
in Appendix 1, the title shall be replaced by the following:
‘Point 28 — Carcinogens: category 1A (Table 3.1)/category 1 (Table 3.2)’;
Appendix 2 shall be amended as follows:
the title shall be replaced by ‘Point 28 — Carcinogens: category 1B (Table 3.1)/ category 2 (Table 3.2)’;
in the entries index Nos 024-017-00-8, 611-024-001, 611-029-00-9, 611-030-00-4 and 650-017-00-8, the words ‘Annex I to Directive 67/548/EEC’ shall be replaced by ‘Annex VI to Regulation (EC) No 1272/2008.’;
in Appendix 3, the title shall be replaced by the following:
‘Point 29 — Mutagens: category 1A (Table 3.1)/category 1 (Table 3.2)’;
in Appendix 4, the title shall be replaced by the following:
‘Point 29 — Mutagens: category 1B (Table 3.1)/category 2 (Table 3.2)’;
in Appendix 5, the title shall be replaced by the following:
‘Point 30 — Reproductive toxicants: category 1A (Table 3.1)/category 1 (Table 3.2)’;
in Appendix 6, the title shall be replaced by the following:
‘Point 30 — Reproductive toxicants: category 1B (Table 3.1)/category 2 (Table 3.2)’;
the word ‘preparation’ or ‘preparations’ within the meaning of Article 3 (2) of Regulation (EC) 1907/2006 shall be replaced by ‘mixture’ or ‘mixtures’ respectively throughout the text.
Article 58 Amendments to Regulation (EC) No 1907/2006 from 1 December 2010
Regulation (EC) No 1907/2006 shall be amended from 1 December 2010 as follows:
in Article 14(4), the introductory sentence shall be replaced by the following:
‘4.If, as a result of carrying out steps (a) to (d) of paragraph 3, the registrant concludes that the substance fulfils the criteria for any of the following hazard classes or categories set out in Annex I to Regulation (EC) No 1272/2008:
(a)hazard classes 2.1 to 2.4, 2.6 and 2.7, 2.8 types A and B, 2.9, 2.10, 2.12, 2.13 categories 1 and 2, 2.14 categories 1 and 2, 2.15 types A to F;
(b)hazard classes 3.1 to 3.6, 3.7 adverse effects on sexual function and fertility or on development, 3.8 effects other than narcotic effects, 3.9 and 3.10;
(c)hazard class 4.1;
(d)hazard class 5.1,
or is assessed to be a PBT or vPvB, the chemical safety assessment shall include the following additional steps:’;
Article 31 shall be amended as follows
paragraph 1(a) shall be replaced by the following:
where a substance meets the criteria for classification as hazardous in accordance with Regulation (EC) No 1272/2008 or a mixture meets the criteria for classification as dangerous in accordance with Directive 1999/45/EC; or’;
paragraph 4 shall be replaced by the following:
‘4.The safety data sheet need not be supplied where substances that are hazardous in accordance with Regulation (EC) No 1272/2008 or mixtures that are dangerous in accordance with Directive 1999/45/EC, offered or sold to the general public, are provided with sufficient information to enable users to take the necessary measures as regards the protection of human health, safety and the environment, unless requested by a downstream user or distributor.’;
Article 40(1) shall be replaced by the following:
‘1.The Agency shall examine any testing proposal set out in a registration or a downstream user report for provision of the information specified in Annexes IX and X for a substance. Priority shall be given to registrations of substances which have or may have PBT, vPvB, sensitising and/or carcinogenic, mutagenic or toxic for reproduction (CMR) properties, or substances above 100 tonnes per year with uses resulting in widespread and diffuse exposure, provided they fulfil the criteria for any of the following hazard classes or categories set out in Annex I of Regulation (EC) No 1272/2008:
(a)hazard classes 2.1 to 2.4, 2.6 and 2.7, 2.8 types A and B, 2.9, 2.10, 2.12, 2.13 categories 1 and 2, 2.14 categories 1 and 2, 2.15 types A to F;
(b)hazard classes 3.1 to 3.6, 3.7 adverse effects on sexual function and fertility or on development, 3.8 effects other than narcotic effects, 3.9 and 3.10;
(c)hazard class 4.1;
(d)hazard class 5.1.’;
Article 57(a), (b) and (c) shall be replaced by the following:
substances meeting the criteria for classification in the hazard class carcinogenicity category 1A or 1B in accordance with section 3.6 of Annex I to Regulation (EC) No 1272/2008;
substances meeting the criteria for classification in the hazard class germ cell mutagenicity category 1A or 1B in accordance with section 3.5 of Annex I to Regulation (EC) No 1272/2008;
substances meeting the criteria for classification in the hazard class reproductive toxicity category 1A or 1B, adverse effects on sexual function and fertility or on development in accordance with section 3.7 of Annex I to Regulation(EC) No 1272/2008;’;
in Article 65 the words ‘Directive 67/548/EEC’ shall be replaced by ‘Directive 67/548/EEC and Regulation (EC) No 1272/2008’;
Article 68(2) shall be replaced by the following:
‘2.For a substance on its own, in a mixture or in an article which meets the criteria for classification in the hazard classes carcinogenicity, germ cell mutagenicity or reproductive toxicity, category 1A or 1B, and could be used by consumers and for which restrictions to consumer use are proposed by the Commission, Annex XVII shall be amended in accordance with the procedure referred to in Article 133(4). Articles 69 to 73 shall not apply.’;
Article 119 shall be amended as follows:
in paragraph 1, point (a) shall be replaced by the following:
without prejudice to paragraph 2(f) and (g) of this Article, the name in the IUPAC nomenclature for substances fulfilling the criteria for any of the following hazard classes or categories set out in Annex I to Regulation (EC) No 1272/2008:
hazard classes 2.1 to 2.4, 2.6 and 2.7, 2.8 types A and B, 2.9, 2.10, 2.12, 2.13 categories 1 and 2, 2.14 categories 1 and 2, 2.15 types A to F;
hazard classes 3.1 to 3.6, 3.7 adverse effects on sexual function and fertility or on development, 3.8 effects other than narcotic effects, 3.9 and 3.10;
hazard class 4.1;
hazard class 5.1.’;
paragraph 2 shall be amended as follows:
point (f) shall be replaced by the following:
subject to Article 24 of Regulation (EC) No 1272/2008, the name in the IUPAC nomenclature for non-phase-in substances referred to in paragraph 1(a) of this Article for a period of six years;’
in point (g), the introductory phrase shall be replaced by the following:
subject to Article 24 of Regulation (EC) No 1272/2008, the name in the IUPAC nomenclature for substances referred to in paragraph 1(a) of this Article that are only used as one or more of the following:’;
in Article 138(1), the second sentence of the introductory phrase shall be replaced by the following:
‘However, for substances meeting the criteria for classification in the hazard classes carcinogenicity, germ cell mutagenicity or reproductive toxicity, category 1A or 1B, in accordance with Regulation (EC) No 1272/2008, the review shall be carried out by 1 June 2014.’;
Annex III shall be amended as follows:
point (a) shall be replaced by the following:
substances for which it is predicted (i.e. by the application of (Q)SARs or other evidence) that they are likely to meet the criteria for category 1A or 1B classification in the hazard classes carcinogenicity, germ cell mutagenicity or reproductive toxicity or the criteria in Annex XIII;’;
in point (b), point (ii) shall be replaced by the following:
for which it is predicted (i.e. by application of (Q)SARs or other evidence) that they are likely to meet the classification criteria for any health or environmental hazard classes or differentiations under Regulation (EC) No 1272/2008.’;
in Annex V, point 8, the words ‘Directive 67/548/EEC’ shall be replaced by ‘Regulation (EC) No 1272/2008’;
in Annex VI, sections 4.1, 4.2 and 4.3 shall be replaced by the following:
‘4.1 The hazard classification of the substance(s), resulting from the application of Title I and II of Regulation (EC) No 1272/2008 for all hazard classes and categories in that Regulation,
In addition, for each entry, the reasons why no classification is given for a hazard class or differentiation of a hazard class should be provided (i.e. if data are lacking, inconclusive, or conclusive but not sufficient for classification),
4.2 The resulting hazard label for the substance(s), resulting from the application of Title III of Regulation (EC) No 1272/2008,
4.3 Specific concentration limits, where applicable, resulting from the application of Article 10 of Regulation (EC) No 1272/2008 and Articles 4 to 7 of Directive 1999/45/EC.’;
Annex VIII shall be amended as follows:
in column 2, the second indent of point 8.4.2 shall be replaced by the following:
‘the substance is known to be carcinogenic category 1A or 1B or germ cell mutagenic category 1A, 1B or 2.’;
in column 2, the second and third paragraphs of point 8.7.1 shall be replaced by the following:
‘If a substance is known to have an adverse effect on fertility, meeting the criteria for classification as toxic for reproduction category 1A or 1B: May damage fertility (H360F), and the available data are adequate to support a robust risk assessment, then no further testing for fertility will be necessary. However, testing for developmental toxicity must be considered.
If a substance is known to cause developmental toxicity, meeting the criteria for classification as toxic for reproduction category 1A or 1B: May damage the unborn child (H360D), and the available data are adequate to support a robust risk assessment, then no further testing for developmental toxicity will be necessary. However, testing for effects on fertility must be considered.’;
in Annex IX, column 2, point 8.7, the second and third paragraphs shall be replaced by the following:
‘If a substance is known to have an adverse effect on fertility, meeting the criteria for classification as toxic for reproduction category 1A or 1B: May damage fertility (H360F), and the available data are adequate to support a robust risk assessment, then no further testing for fertility will be necessary. However, testing for developmental toxicity must be considered.
If a substance is known to cause developmental toxicity, meeting the criteria for classification as toxic for reproduction category 1A or 1B: May damage the unborn child (H360D), and the available data are adequate to support a robust risk assessment, then no further testing for developmental toxicity will be necessary. However, testing for effects on fertility must be considered.’;
Annex X shall be amended as follows:
in column 2, point 8.7, the second and third paragraphs shall be replaced by the following:
‘If a substance is known to have an adverse effect on fertility, meeting the criteria for classification as toxic for reproduction category 1A or 1B: May damage fertility (H360F), and the available data are adequate to support a robust risk assessment, then no further testing for fertility will be necessary. However, testing for developmental toxicity must be considered.
If a substance is known to cause developmental toxicity, meeting the criteria for classification as toxic for reproduction category 1A or 1B: May damage the unborn child (H360D), and the available data are adequate to support a robust risk assessment, then no further testing for developmental toxicity will be necessary. However, testing for effects on fertility must be considered.’
in column 2, point 8.9.1, the second indent of the first paragraph shall be replaced by the following:
‘the substance is classified as germ cell mutagen category 2 or there is evidence from the repeated dose study(ies) that the substance is able to induce hyperplasia and/or pre-neoplastic lesions.’
in column 2, the second paragraph of point 8.9.1 shall be replaced by the following:
‘If the substance is classified as germ cell mutagen category 1A or 1B, the default presumption would be that a genotoxic mechanism for carcinogenicity is likely. In these cases, a carcinogenicity test will normally not be required.’;
in Annex XIII, the second and third indents of point 1.3 shall be replaced by the following:
‘the substance is classified as carcinogenic (category 1A or 1B), germ cell mutagenic (category 1A or 1B), or toxic for reproduction (category 1A, 1B or 2), or
there is other evidence of chronic toxicity, as identified by the classifications STOT (repeated exposure), category 1 (oral, dermal, inhalation of gases/vapours, inhalation of dust/mist/fume) or category 2 (oral, dermal, inhalation of gases/vapours, inhalation of dust/mist/fume) according to Regulation (EC) No 1272/2008’;
in the table in Annex XVII, the column ‘Designation of the substance, of the groups of substances or of the mixture’ shall be amended as follows:
entry 3 shall be replaced by the following:
‘3. Liquid substances or mixtures which are regarded as dangerous in accordance with Directive 1999/45/EC or are fulfilling the criteria for any of the following hazard classes or categories set out in Annex I to Regulation (EC) No 1272/2008:
hazard classes 2.1 to 2.4, 2.6 and 2.7, 2.8 types A and B, 2.9, 2.10, 2.12, 2.13 categories 1 and 2, 2.14 categories 1 and 2, 2.15 types A to F;
hazard classes 3.1 to 3.6, 3.7 adverse effects on sexual function and fertility or on development, 3.8 effects other than narcotic effects, 3.9 and 3.10;
hazard class 4.1;
hazard class 5.1.’;
entry 40 shall be replaced by the following:
‘40. Substances classified as flammable gases category 1 or 2, flammable liquids categories 1, 2 or 3, flammable solids category 1 or 2, substances and mixtures which, in contact with water, emit flammable gases, category 1, 2 or 3, pyrophoric liquids category 1 or pyrophoric solids category 1, regardless of whether they appear in Part 3 of Annex VI to that Regulation or not’.
Article 59 Amendments to Regulation (EC) No 1907/2006 from 1 June 2015
Regulation (EC) No 1907/2006 shall be amended from 1 June 2015 as follows:
Article 14(2) shall be replaced by the following:
‘2.A chemical safety assessment in accordance with paragraph 1 need not be performed for a substance which is present in a mixture if the concentration of the substance in the mixture is less than
(a)the cut-off value referred to in Article 11, paragraph 3 of Regulation (EC) No 1272/2008;
(b)0,1 % weight by weight (w/w), if the substance meets the criteria in Annex XIII to this Regulation.’;
Article 31 shall be amended as follows:
in paragraph 1, point (a) shall be replaced by the following:
where a substance or mixture meets the criteria for classification as hazardous in accordance with Regulation (EC) No 1272/2008; or’;
paragraph 3 shall be replaced by the following:
‘3.The supplier shall provide the recipient at his request with a safety data sheet compiled in accordance with Annex II, where a mixture does not meet the criteria for classification as hazardous in accordance with Titles I and II of Regulation (EC) No 1272/2008, but contains:
(a)in an individual concentration of ≥ 1 % by weight for non-gaseous mixtures and ≥ 0,2 % by volume for gaseous mixtures at least one substance posing human health or environmental hazards; or
(b)in an individual concentration of ≥ 0,1 % by weight for non-gaseous mixtures at least one substance that is carcinogenic category 2 or toxic to reproduction category 1A, 1B and 2, skin sensitiser category 1, respiratory sensitiser category 1, or has effects on or via lactation or is persistent, bioaccumulative and toxic (PBT) in accordance with the criteria set out in Annex XIII or very persistent and very bioaccumulative (vPvB) in accordance with the criteria set out in Annex XIII or has been included for reasons other than those referred to in point (a) in the list established in accordance with Article 59(1); or
(c)a substance for which there are Community workplace exposure limits’;
paragraph 4 shall be replaced by the following:
‘4.The safety data sheet need not be supplied where hazardous substances or mixtures offered or sold to the general public are provided with sufficient information to enable users to take the necessary measures as regards the protection of human health, safety and the environment, unless requested by a downstream user or distributor.’;
Article 56(6)(b) shall be replaced by the following:
for all other substances, below the values specified in Article 11(3) of Regulation (EC) No 1272/2008 which result in the classification of the mixture as hazardous.’;
in Article 65 the words ‘and Directive 1999/45/EC’ shall be deleted;
Annex II shall be amended as follows:
point 1.1 shall be replaced by:
‘1.1. Identification of the substance or mixture
The term used for identification of a substance shall be identical to that provided on the label in accordance with Article 18(2) of Regulation (EC) No 1272/2008.
The term used for identification of a mixture shall be identical to that provided on the label in accordance with Article 18(3)(a) of Regulation (EC) No 1272/2008.’;
footnote 1 to point 3.3(a), first indent, shall be deleted;
point 3.6 shall be replaced by:
‘3.6. Where, in accordance with Article 24 of Regulation (EC) No 1272/2008, the Agency has agreed that the chemical identity of a substance may be kept confidential on the label and in the safety data sheet, their chemical nature shall be described under heading 3 in order to ensure safe handling.
The name used on the safety data sheet (including for the purposes of paragraphs 1.1, 3.2, 3.3 and 3.5) shall be the same as that used on the label, agreed in accordance with the procedure set out in Article 24 of Regulation (EC) No 1272/2008.’;
in Annex VI section 4.3 shall be replaced by the following:
‘4.3 Specific concentration limits, where applicable, resulting from the application of Article 10 of Regulation (EC) No 1272/2008.’;
Annex XVII shall be amended as follows:
in the column ‘Designation of the substance, of the groups of substances or of the mixture’ of the table in entry 3, the words ‘which are regarded as dangerous in accordance with Directive 1999/45/EC or are’ shall be deleted;
in the column ‘Conditions of restriction’ of the table, entry 28 shall be amended as follows:
the second indent of point 1 shall be replaced by the following:
‘the relevant generic concentration limit specified in Part 3 of Annex I of Regulation (EC) No 1272/2008.’;
point 2 (d) shall be replaced by the following:
artists’ paints covered by Regulation (EC) No 1272/2008’.
F132Article 60 Repeal
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F133Article 61 Transitional provisions
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F134Article 62 Entry into force
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This Regulation shall be binding in its entirety and directly applicable in all Member States.