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Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Use these forms if you import, export, or move goods through the UK.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
Pharmacovigilance system requirements
Guidance for businesses.
Form to report patients meeting the case definition.
Check the tariff classification for dried buffalo ears and dried beef meat scraped off from the throat, for use as animal feed.
Export controls on goods that can be used for torture or capital punishment.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Imposing safeguard measures for imports of certain steel products.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Use this form to file a translation in connection with a European patent or a European patent application
The National Archives is the official archive and publisher for the UK government and for England and Wales. It is the guardian of some of our most iconic national documents, dating back over 1,000 years. The National Archives is a...
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
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