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Pharmacovigilance system requirements
Register as a manufacturer, importer or distributor of active substances.
Information about the EU Regulations and their implementation in Northern Ireland
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
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.
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
Look up a trade mark to see if something identical or similar to your brand is already registered.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
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.
What you need to do to work and operate in the aviation industry.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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
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