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How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to apply for marketing authorisation via this new procedure.
How to use a case-control study to evaluate your digital health product.
Apply for a higher education course, track your application and accept or reject your offers.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
This guide provides information on statutory derecognition of a trade union
Find out which birds and animals may be spared from culling during an outbreak of an exotic animal disease.
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Volume 36 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
Information for patients, healthcare professionals and developers of new medicines
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
How to use A/B testing to evaluate your digital health product.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Volume 38 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
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