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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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.
How to register if you keep 50 or more birds, including any you keep as pets.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Website of Colchester City Council
Learn how to check if your website or mobile app is accessible.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to develop a management system and keep it up to date so that you can carry out activities under an environmental permit.
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