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How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How you can report cases of modern slavery in the UK if you’re a first responder.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Actions that trial sponsors should consider to build resilience into clinical trial design
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Lassa virus causes Lassa fever, an acute viral haemorrhagic fever (VHF).
How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
The AQuA Book is Government guidance about how to produce robust, fit for purpose analysis. It's for all analysts, analytical managers and commissioners.
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