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How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Comply with good pharmacovigilance practice and prepare for an inspection.
From discovery to real-world impact, VDEC equips scientists with the expertise and facilities to navigate each step in the development of vaccines and therapeutics.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Keep up to date with the latest information from the UK GLP monitoring authority.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
This guidance explains what .gov.uk agreements Registrars, Registrant and sub-Registrants need in place to protect their .gov.uk domains.
Find out about our Export Development Guarantee: its benefits, eligibility criteria and how to apply.
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