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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Report examining issues relating to road safety and the use and prescription of medical cannabis.
Call for evidence to support ACMD's review of changes to legislation on the use of cannabis-based products for medicinal purposes (CBPMs).
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
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