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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
FCDO travel advice for Curaçao. Includes safety and security, insurance, entry requirements and legal differences.
FCDO travel advice for St Maarten. Includes safety and security, insurance, entry requirements and legal differences.
Using metadata to make it easier to catalogue, validate, reuse and share your data.
FCDO travel advice for Brazil. Includes safety and security, insurance, entry requirements and legal differences.
FCDO travel advice for Côte d'Ivoire. Includes safety and security, insurance, entry requirements and legal differences.
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