Medicines and Medical Devices Act 2021

Information

Type

Regulation

Regulated products

Medical Devices

Published

February 11, 2021

Last updated

February 11, 2021

Description

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.

Organization

Country / Region

United Kingdom

License

Open Government Licence 3.0 (United Kingdom)

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