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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
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 get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to use a cost utility analysis to evaluate your digital health product.
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.
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 show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to apply for marketing authorisation via this new procedure.
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 case-control study to evaluate your digital health product.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
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