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An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
This guidance is an introduction to the Open Document Format (ODF) standard and how you can select ODF-compliant solutions.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Use this form to file a translation in connection with a European patent or a European patent application
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 choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Check how much your visa application costs in the country you’re in
Student visa - check which courses you can study, prepare supporting documents, apply, what happens at the UK border
Short-term study visa - prepare supporting documents, apply, book and attend an appointment, what happens at the UK border
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Find a supplier who can provide user research participants to test your service with.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
The Multidisciplinary University Research Initiative (MURI) is a US Department of Defense (DoD) programme.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
This is advice for UK sponsors whose students are affected by coronavirus (COVID-19).
Don’t include personal or financial information like your National Insurance number or credit card details.
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