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Apply for a UK Ancestry visa if you're a Commonwealth citizen and can prove that one of your grandparents was born in the UK - eligibility, fees, documents, how to apply, how long it takes and how to settle
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Pharmacovigilance system requirements
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
Check how much your visa application costs in the country you’re in
Make sure that domains that do not send email cannot be used for spoofing.
The National Archives is the official archive and publisher for the UK government and for England and Wales. It is the guardian of some of our most iconic national documents, dating back over 1,000 years. The National Archives is a...
How to contact MHRA for specific services or enquiries.
Use this form to file a translation in connection with a European patent or a European patent application
Look up a trade mark to see if something identical or similar to your brand is already registered.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
A CV is a summary of your skills, achievements and experience that you use to apply for jobs. Check advice on what to include and how to make it stand out.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
How to get fast-track approval of medical devices during COVID-19.
How to use A/B testing to evaluate your digital health product.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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