Policy paper – Report on regulations made under sections 2(1), 10(1), 15(1) and 19(1) of the Medicines and Medical Devices Act 2021
Presented to Parliament pursuant to section 46(1) of the Medicines and Medical Devices Act 2021.
The Medicines and Medical Devices Act (MMDA) became law in February 2021. The act provides the Secretary of State for Health and Social Care and the Department of Health in Northern Ireland with powers to amend the existing regulations on human and veterinary medicines, as well as medical devices in the UK. The MMDA allows the UK to change the regulatory landscape for medicines and medical devices following our departure from the EU.
Published on the 29th of february 2024. Read the entire news report following this link.
OpenEdition vous propose de citer ce billet de la manière suivante :
adelage (21 mai 2024). Policy paper – Report on regulations made under sections 2(1), 10(1), 15(1) and 19(1) of the Medicines and Medical Devices Act 2021. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/11p1b





