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How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Information for manufacturers.
Pharmacovigilance system requirements
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Find out what records you must keep and how to keep them if you're registered for VAT.
Information about the EU Regulations and their implementation in Northern Ireland
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Use a separate statement of objection form for each Japanese GI product name you object to.
Check how much your visa application costs in the country you’re in
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Information on mass, length and volume calibration for local authorities.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
How to legally run a business that deals with the wholesale of animal medicines (veterinary medicinal products) and the WDA Register.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
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
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.
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.
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