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How to prepare for implementation and compliance of the Safety Features Regulation.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Check the tariff classification for a defined daily dose of active substances.
Industry must notify the MHRA if they will not be using these flexibilities
Tougher sentences for cowardly killers delivered a year on from Wade Review.
The MHRA has today set out its strategic approach to artificial intelligence (AI)
How to apply for access to personal data from DfE and its executive agencies.
Notices of publication and a consolidated list of references of pre-Exit European Assessment Documents for construction products.
Find out about the legal definitions of biofuel products, excise duty rates and the roles and responsibilities of producers from 1 April 2022.
Published standards for regulatory work 2023/24
We are producing guidance and information for industry, healthcare professionals and patients covering the coronavirus (COVID-19) outbreak.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Guidance for industry and organisations to follow from 1 January 2021.
This series brings together all documents relating to forensic science.
Guidance on Defence and Security Accelerator terms and conditions for funding, contracts and intellectual property rights.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
Field inspection reports for the Genetic Modification Inspectorate deliberate release inspection programme in England.
Statistical notice about changes to the way DWP will publish statistics about benefit underpayments and how it will classify cases which fail to provide evidence.
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