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Use this page to verify Certificates of Competency (CoC) and Flag State Endorsements (FSE) online.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Pharmacovigilance system requirements
Actions that trial sponsors should consider to build resilience into clinical trial design
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Use this form to file a translation in connection with a European patent or a European patent application
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.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
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
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
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.
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.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
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