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Departments, agencies and public bodies
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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
This series brings together all documents relating to Guidance and methods
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on applications for a UK visa or visa extension under Global Talent.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guidance on various aspects of the planning system, given in letters to chief planning officers of local planning authorities.
A collection of active marine guidance notes, published by the Maritime and Coastguard Agency (MCA).
Vessel traffic management, electronic nautical publications and safety information for owners, operators of ships, yachts, fishing vessels.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Visas and immigration operational guidance for staff.
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