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How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Pharmacovigilance system requirements
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Find the address, contact details and opening times of the UK visa application centre for your country.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
The Civil Aviation Authority (CAA) is responsible for the regulation of aviation safety in the UK, determining policy for the use of airspace, the economic regulation of Heathrow, Gatwick and Stansted airports, the licensing and financial fitness of airlines and...
What you need to do to work and operate in the aviation industry.
AVU provides services for genotypic antiviral resistance testing of HIV and HCV, investigation of HIV transmission events and HSV antiviral resistance testing by phenotyping.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Information and advice on rabies, the viral infection of the central nervous system which affects mammals and humans.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Use a separate statement of objection form for each Japanese GI product name you object to.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
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
Regulations to reduce the risk posed by the production, importation and storage of ammonium nitrate.
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