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Southern Region, Valuer Chair R Waterhouse FRICS, Ms C Barton MRICS and Ms J Dalal on 18 October 2024
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Submission dates and how the submissions using the EC decision reliance procedure work.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
What users need to know to know about the Taking Part survey.
Why data relating to EPCs will be made available and how individuals can opt out of having their data disclosed publicly.
Information on how the CMA investigated the merger, and how you can find out more.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
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