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 18 work packageable things.

Work packageable things per page: 20 50 100

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

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

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

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

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

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

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

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

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

10. Veterinary Medicines (Amendment etc.) Regulations 2024

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

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

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

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

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

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

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

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

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