“medicinal product”

1. Access to Medical Treatments (Innovation) Act 2016 Act
2. Communications Act 2003 Act
3. The Consumer Contracts (Information, Cancellation and Additional Charges) Regulations 2013 SI
4. The Control of Poisons and Explosives Precursors Regulations 2015 SI
5. Criminal Law (Consolidation) (Scotland) Act 1995 Act
6. Criminal Procedure (Scotland) Act 1995 Act
7. Digital Markets, Competition and Consumers Act 2024 Act
8. The Environmental Protection (Prescribed Processes and Substances) Regulations 1991 SI
9. Finance Act 2021 Act
10. Finance Act 2026 Act
11. The General Product Safety Regulations 2005 SI
12. Health Act 1999 Act
13. The Human Medicines Regulations 2012 SI 2 definitions
14. Licensing Act 2003 Act
15. The Medical Devices Regulations 2002 SI 2 definitions
16. Medicines Act 1968 Act
17. Medicines Act 1971 Act
18. The Medicines (Aristolochia and Mu Tong etc.) (Prohibition) Order 2001 SI
19. The Medicines (Aristolochia and Mu Tong etc.) (Temporary Prohibition) Order 2000 SI
20. The Medicines (Exemptions and Miscellaneous Amendments) Order 2009 SI 2 definitions
21. The Medicines for Human Use (Clinical Trials) Regulations 2004 SI
22. The Medicines for Human Use (Kava-kava) (Prohibition) Order 2002 SI
23. The Medicines for Human Use (Prescribing by EEA Practitioners) Regulations 2008 SI 2 definitions
24. The Medicines for Human Use (Prescribing) Order 2005 SI
25. The Medicines (Products for Human Use-Fees) Regulations 2008 SI 2 definitions
26. The Medicines (Products for Human Use) (Fees) Regulations 2016 SI 2 definitions
27. The Misuse of Drugs (Designation) (England, Wales and Scotland) Order 2015 SI
28. The Misuse of Drugs Regulations 2001 SI
29. National Health Service Act 2006 Act
30. The National Health Service (General Medical Services Contracts) Regulations 2015 SI
31. The National Health Service (Personal Medical Services Agreements) Regulations 2015 SI
32. The Nicotine Inhaling Products (Age of Sale and Proxy Purchasing) Regulations 2015 SI
33. The Notification of Deaths Regulations 2019 SI
34. Offender Management Act 2007 Act
35. Patents Act 1977 Act 2 definitions
36. The Pharmacy Order 2010 SI 2 definitions
37. Prison Act 1952 Act
38. The Producer Responsibility Obligations (Packaging and Packaging Waste) Regulations 2024 SI
39. Psychoactive Substances Act 2016 Act
40. Rare Cancers Act 2026 Act
41. Regulation (EC) No 469/2009 of the European Parliament and of the Council of 6 May 2009 concerning the supplementary protection certificate for medicinal products (Codified version) (Text with EEA relevance) EU regulation
42. Regulation (EU) 2019/125 of the European Parliament and of the Council of 16 January 2019 concerning trade in certain goods which could be used for capital punishment, torture or other cruel, inhuman or degrading treatment or punishment (codification) EU regulation
43. Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC (Text with EEA relevance) EU regulation
44. The Security of Animal Pathogens (Exceptions to Dangerous Substances) Regulations 2007 SI
45. The Security of Pathogens and Toxins (Exceptions to Dangerous Substances) Regulations 2002 SI
46. Sunday Trading Act 1994 Act
47. The Tobacco and Related Products Regulations 2016 SI
48. Tobacco and Vapes Act 2026 Act 2 definitions
49. The Unlicensed Medicinal Products for Human Use (Transmissible Spongiform Encephalopathies) (Safety) Regulations 2003 SI
50. Value Added Tax Act 1994 Act
51. The Waste Electrical and Electronic Equipment Regulations 2013 SI

Definitions are taken from the instruments as published on zoomLaw, for guidance only. Check the instrument itself for its scope and any amendments.