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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 use a quasi-experimental study to evaluate your digital health product.
A new expert panel chaired by Deputy Prime Minister David Lammy will meet for the first time today (Monday 8 December), to make sure the UK remains a leading global centre for legal services.
You can make observations on the patentability of a published patent application.
How to use a before-and-after study to evaluate your digital health product.
UK guideline on GMP for decentralised manufacturing, ensuring compliance with EU GMP principles for safe, quality medicinal products.
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.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
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