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How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
UK guideline on GMP for decentralised manufacturing, ensuring compliance with EU GMP principles for safe, quality medicinal products.
Upper Tribunal Administrative Appeals Chamber decision by Judge Caldwell on 29 December 2025.
How to use a quasi-experimental study to evaluate your digital health product.
How to use a before-and-after study to evaluate your digital health product.
Good Practice Guide (GPG) 45 helps you decide how to check someone's identity.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Guidance for clinical trials that use Decentralised Manufactured Investigational Medicinal Products (IMPs).
Comply with good pharmacovigilance practice and prepare for an inspection.
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