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How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
How to use an ethnographic study to evaluate your digital health product.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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