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More informationVeterinary Medicines Website
UK Government response to consultation on the future regulation of medical devices in the United Kingdom
Laboratories that are members of the UK GLP Compliance Monitoring Programme as of 28 June 2022
UK to strengthen regulation of medical devices to protect patients
UK Gov - The Future of Clinical Research Delivery: 2022-2025 Implementation Plan
Why involve the public in research?
FDA released 'Safety Considerations for Container Labels and Carton Labelling Design to Minimise Medication Errors' in May 2022.
MHRA joins International Medical Device Regulatory Forum, the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use and the Medical Devices Innovation Consortium.
The European Commission have released a Q&A document concerning Complex Clinical Trials.
Human Medicines Highlights Newsletter, June 2022 released