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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.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
FCDO travel advice for Trinidad and Tobago. Includes safety and security, insurance, entry requirements and legal differences.
Before you travel No travel can be guaranteed safe. Read all the advice in…
This information is for people travelling on a full ‘British citizen’…
Terrorism There is a high threat of terrorist attack globally affecting UK…
Before you travel check that: your destination can provide the healthcare…
The Foreign, Commonwealth & Development Office (FCDO) cannot provide…
Apply for a Temporary Work – International Agreement visa if you're working under international law (including diplomatic households) - extend or switch, family members
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
How to use a before-and-after study to evaluate your digital health product.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Blogs where government organisations talk about their work and share information and ideas.
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