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Data, Freedom of Information releases and corporate reports
What to do if you think you've spotted a scam pretending to be from Companies House, and examples of scam emails, letters and telephone calls.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
Submissions related to human medicines need to be submitted directly to the MHRA.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Learn how to check if your website or mobile app is accessible.
Blogs where government organisations talk about their work and share information and ideas.
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