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Pharmacovigilance system requirements
Check how much your visa application costs in the country you’re in
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Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Use this form to file a translation in connection with a European patent or a European patent application
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
How contracting authorities can find approved specialist providers and award contracts for decontamination services in relation to a CBRN or major HazMat incident.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
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
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Find a supplier who can provide user research participants to test your service with.
Check the patents journal to find UK-registered patents granted, published and filed
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
How to get fast-track approval of medical devices during COVID-19.
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