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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on whether or not your product is a medical device.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
First published during the 2022 to 2024 Sunak Conservative government
Today (30 April 2024), the Government is strengthening its trade border to better detect pests and diseases from imported products.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
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