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Use this form to file a translation in connection with a European patent or a European patent application
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
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 form C88 (status) as proof of authorisation to import or export for the country of destination.
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...
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
The requirements for packaging DNLEU
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
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
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.
Find out how to do a rapid lateral flow test for COVID-19. Rapid lateral flow tests show the result on a device that comes with the test.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Calculate value build-up costs for use with the Single Administrative Document (SAD) using form C89.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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