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Medicines and Medical Devices Act 2021 (Chapter 3 of 2021).

Pays/Territoire
Royaume-Uni
Type du document
Législation
Date
2021
Source
FAO, FAOLEX
Titre complet
An Act to make provision about a Commissioner for Patient Safety in relation to human medicines and medical devices; confer power to amend or supplement the law relating to human medicines, veterinary medicines and medical devices; make provision about the enforcement of regulations, and the protection of health and safety, in relation to medical devices; and for connected purposes.
Sujet
Bétail, Général
Mot clé
Santé publique Accès-à-l'information Santé des animaux Institution Infractions/sanctions Médicaments
Aire géographique
Îles de l'Océan Atlantique, Europe, Europe et Asie Centrale, Atlantique Nord, Mer du Nord, Atlantique du Nord-Est, Europe du Nord
Résumé

The Medicines and Medical Devices Act 2021 (the Act): 1) establishes a Patient Safety Commissioner, with the core duties of promoting patient safety and the importance of the patient voice in relation to the regulation of human medicines and medical devices; 2) introduces targeted delegated powers in the fields of human medicines, veterinary medicines and medical devices to enable the existing regulatory frameworks to be updated following the United Kingdom’s (UK) departure from the European Union (EU); 3) provides information sharing gateways to enabling sharing with outside of the UK in order to give effect to international agreements and arrangements concerning the regulation of human medicines, veterinary medicines and medical devices; 4) provides a delegated power to establish one or more information systems in relation to medical devices; 5) provides a delegated power to establish on a legislative basis a medical device expert advisory committee; 6) and consolidates the enforcement provisions for medical devices and introduces civil sanctions.

Texte intégral
Anglais
Site web
www.legislation.gov.uk