Medicines and Medical Devices Act 2021

2021 c. 3. An Act of Parliament gaining Royal Assent on 11 February 2021.

Read the enabling legislation at legislation.gov.uk.

There are 19 work packageable things.

Work packageable things per page: 20 50 100

1. Human Medicines (Amendments Relating to Hub and Spoke Dispensing etc.) Regulations 2025

2. Medical Devices and Blood Safety and Quality (Fees Amendment) Regulations 2025

3. Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2025

4. Medical Devices (Amendment) (Great Britain) Regulations 2025

5. Medicines for Human Use (Clinical Trials) (Amendment) Regulations 2024

6. Human Medicines (Amendment) (Modular Manufacture and Point of Care) Regulations 2024

7. Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024

8. Human Medicines (Amendments Relating to Naloxone and Transfers of Functions) Regulations 2024

9. Human Medicines (Amendments relating to Registered Dental Hygienists, Registered Dental Therapists and Registered Pharmacy Technicians) Regulations 2024

10. Veterinary Medicines (Amendment etc.) Regulations 2024

11. Human Medicines (Amendments Relating to Coronavirus and Influenza) (England and Wales and Scotland) Regulations 2024

12. Human Medicines (Amendment Relating to Original Pack Dispensing) (England and Wales and Scotland) Regulations 2023

13. Medical Devices (Amendment) (Great Britain) Regulations 2023

14. Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2023

15. Medical Devices and Blood Safety and Quality (Fees Amendment) Regulations 2023

16. Human Medicines (Amendments Relating to the Early Access to Medicines Scheme) Regulations 2022

17. Commissioner for Patient Safety (Appointment and Operation) (England) Regulations 2022

18. Human Medicines (Coronavirus and Influenza) (Amendment) Regulations 2022

19. Medical Devices (Coronavirus Test Device Approvals) (Amendment) Regulations 2021

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