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Guidance for applying for a Deck CoC for Commercial and Private Yachts.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
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.
Website of Colchester Borough Council
Resources for individuals and organisations to use supporting a variety of safety awareness campaigns.
Details of how Marketing Authorisation Holders can provide information on planned or potential future submissions, to the MHRA.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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