Statutory Instruments
2000 No. 1368
MEDICINES
The Medicines (Aristolochia and Mu Tong etc. ) (Temporary Prohibition) Order 2000
Made
18th May 2000
Laid before Parliament
19th May 2000
Coming into force
16th June 2000
As respects England, Scotland and Wales, the Secretary of State concerned with health in England, and, as respects Northern Ireland, the Department of Health, Social Services and Public Safety, acting jointly, in exercise of the powers conferred upon them by sections 62(1)(a) and (2) and 129(4) of the Medicines Act 1968( 1 ) and now vested in them( 2 ) and of all other powers enabling them in that behalf, it appearing to them to be necessary in the interests of safety to make the following Order, after consulting such organisations as appear to them to be representative of interests likely to be substantially affected by the Order pursuant to section 129(6) of that Act, after consulting and taking into account the advice of the Committee on Safety of Medicines pursuant to sections 62(3) and 129(7) of that Act( 3 ), and after taking into account the report of the Medicines Commission made under section 62(5) of that Act, hereby make the following Order:—
Citation, commencement, expiry and interpretation
1. —(1) This Order may be cited as the Medicines (Aristolochia and Mu Tong etc.) (Temporary Prohibition) Order 2000, shall come into force on 16th June 2000 and shall continue in force until the end of 30th June 2001, when it shall expire.
(2) In this Order—
“the Act” means the Medicines Act 1968;
“EEA Agreement” means the Agreement on the European Economic Area signed at Oporto on 2nd May 1992( 4 ) as adjusted by the Protocol signed at Brussels on 17th March 1993( 5 );
“EEA State” means a State which is a Contracting Party to the EEA Agreement;
“medicinal product” does not include a medicinal product which is a veterinary drug.
Prohibition of sale, supply and importation of any medicinal product consisting of or containing certain plants
2. Subject to article 4 below, the sale, supply and importation of any medicinal product consisting of or containing a plant( 6 ) —
(a) belonging to a species of the genus Aristolochia ; or
(b) belonging to any of the species—
Akebia quinata,
Akebia trifoliata,
Clematis armandii,
Clematis montana,
Cocculus laurtfolius,
Cocculus orbiculatus,
Cocculus trilobus,
Stephania tetrandra,
or consisting of or containing an extract from such a plant, is prohibited.
Prohibition of sale, supply and importation of any medicinal product presented as consisting of or containing Mu Tong etc.
3. Subject to article 4 below, the sale, supply and importation of any medicinal product is prohibited where, at the time of the sale, supply or importation—
(a) the label on the product’s container or package; or
(b) any document accompanying the product,
indicates in any language—
(i) that the product consists of or contains Mu Tong or Fangji , or any term derived from either of those terms; or
(ii) that the product consists of or contains a plant specified in article 2(b) above or an extract from such a plant.
Exceptions to the prohibitions imposed by articles 2 and 3 above
4. —(1) The prohibitions imposed by articles 2 and 3 above are subject to the exceptions specified in the following paragraphs of this article.
(2) The prohibitions imposed by articles 2 and 3 above shall not apply where a medicinal product as referred to in those articles is sold or supplied to, or, in the case of importation, is imported by or on behalf of, any of the following persons—
(a) a food analyst or food examiner within the meaning of section 30 of the Food Safety Act 1990( 7 );
(b) a food analyst or food examiner within the meaning of Article 30 or 31 of the Food Safety (Northern Ireland) Order 1991( 8 );
(c) an authorised officer within the meaning of section 5(6) of the Food Safety Act 1990, or Article 2(2) of the Food Safety (Northern Ireland) Order 1991( 9 );
(d) a person duly authorised by an enforcement authority under sections 111 and 112 of the Act;
(e) a sampling officer within the meaning of Schedule 3 to the Act.
(3) The prohibitions on importation imposed by articles 2 and 3 above shall not apply where a medicinal product as referred to in those articles is imported—
(a) from a member State of the European Community; or
(b) where the product originates( 10 ) in the European Economic Area, from an EEA State which is not also a member State of the European Community.
(4) The prohibitions imposed by articles 2 and 3 above shall not apply where a medicinal product as referred to in those articles is the subject of a product licence( 11 ), a marketing authorization within the meaning of regulation 1(4)(a) of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994( 12 ) or a certificate of registration within the meaning of regulation 1(2) of the Medicines (Homoeopathic Products for Human Use) Regulations 1994( 13 ).
Revocation
5.The Medicines (Aristolochia) (Temporary Prohibition) Order 1999( 14 ) is revoked.
Signed by authority of the Secretary of State for Health
Hunt
Parliamentary Under Secretary of State,
Department of Health
18th May 2000
Sealed with the Official Seal of the Department of Health, Social Services and Public Safety on 18th May 2000.
L.S.
D. A. Baker
A Senior Officer of the
Department of Health, Social Services and Public Safety
1968 c. 67 ; the expressions “the appropriate Ministers” and “the Health Ministers” are defined in section 1 of that Act as amended by article 2(2) of, and Schedule 1 to, S.I. 1969/388 , and by articles 2(1) and 5 of, and the Schedule to, S.I. 1999/3142 .
In the case of the Secretary of State concerned with health in England, by virtue of article 2(2) of, and Schedule 1 to, S.I. 1969/388 , and articles 2(1) and 5 of, and the Schedule to, S.I. 1999/3142 ; in the case of the Department of Health, Social Services and Public Safety, the powers vested in the Minister in charge of that Department by virtue of section 95(5) of, and paragraph 10 of Schedule 12 to, the Northern Ireland Act 1998 (c. 47) may now be exercised by the Department by virtue of section 1(8) of, and paragraph 4(1)(b) of the Schedule to, the Northern Ireland Act 2000 (c. 1) ; the Department was named with its present name by virtue of article 3(b) of S.I. 1999/283 (N.I. 1) .
Section 62(3) refers to “the appropriate committee”, which is defined in section 4(6) of the Act. The Committee on Safety of Medicines was established under section 4 of the Act, by S.I. 1970/1257 , for the purposes set out in that instrument.
OJ No. L1, 3.1.94, p. 3.
OJ No. L1, 3.1.94, p. 572.
“Plant” includes part of a plant; see section 132(1) of the Act.
1990 c. 16 : section 30 was amended by section 40 of, and paragraph 8 of Schedule 5 to, the Food Standards Act 1999 (c. 28) .
S.I. 1991/762 (N.I. 7) ; as amended by S.I. 1996/1633 (N.I. 12) .
Section 5(b) was amended by section 40 of, and paragraph 8 of Schedule 5 to, the Food Standards Act 1999; article 2(2) was amended by paragraph 29 of Schedule 5 to, and Schedule 6 to, that Act.
See Protocol 4 (on rules of origin) annexed to the EEA Agreement, as amended by the Decision of the EEA Joint Committee No. 6/94 amending Protocol 4 to the EEA Agreement (OJ No. L95, 14.4.94, p. 22).
“Product licence” has the meaning assigned to it by section 7 of the Act.
S.I. 1994/105 ; as amended by S.I. 1994/899 , 1995/541 , 1996/482 , 1998/574 , 1999/566 and 2000/592 .
S.I. 1999/2889 .