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Data, Freedom of Information releases and corporate reports
Information to support your recovery after COVID-19.
Guidance and support on coronavirus (COVID-19) in Scotland.
Submission dates and how the submissions using the EC decision reliance procedure work.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
How to use a cost benefit analysis to evaluate your digital health product.
Guidance and support on coronavirus (COVID-19) in Wales.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Blogs where government organisations talk about their work and share information and ideas.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to apply for marketing authorisation via this new procedure.
How to conform with the legal requirements for placing medical devices on the market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Clinicians are provided with actions to complete when managing infectious diseases in the asylum seeker population.
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