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Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
Diseases and health problems in sheep and goats, including foot and mouth disease (FMD), scrapie and lead poisoning
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
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.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to use A/B testing to evaluate your digital health product.
Find details of recent trade mark applications or amendments by searching the journal
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Urgent public health message: UKHSA has been notified about an outbreak of food botulism in France involving a small number of British nationals.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information and guidance on a range of medical devices for users and patients.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
How to get fast-track approval of medical devices during COVID-19.
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
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