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Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
A collection of investigatory reports published by the National Measurement and Regulation Office Enforcement Services.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
CMA interim report highlights persistent issues in the civil engineering market for roads and railways – which appear to hinder UK growth and productivity.
Guidance covering various aspects of pharmacovigilance for authorised and unauthorised medicinal products (Specials and the Early Access to Medicines Scheme (EAMS)).
Accounts of the review of systemic and wider issues arising from Iraq and other military operations.
How the Competition and Markets Authority's (CMA) market study is taking place, and how you can engage with it.
MHRA’s mechanism for evaluating the justifications supplied by applicant organisations who plan to utilise decentralised manufacture.
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