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Pharmacovigilance system requirements
Check how much your visa application costs in the country you’re in
The civil procedure rules govern the way civil cases are managed, and set out the processes of the Civil Division of the Court of Appeal, the High Court and the County Court.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
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...
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Use this form to file a translation in connection with a European patent or a European patent application
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
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
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Find out about local procedures, burials and cremations, and returning the body to the UK.
Application pack to get a certificate of custom and law for marriage in Belgium by post.
Official information for UK nationals living in or moving to Belarus, including guidance on residency, passports and healthcare.
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.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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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