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Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Use these forms if you import, export, or move goods through the UK.
Marburg virus is a Filovirus which, along with Ebola virus, can cause a severe and often fatal viral haemorrhagic fever (VHF).
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Check how much your visa application costs in the country you’re in
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
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...
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Look up a trade mark to see if something identical or similar to your brand is already registered.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
The requirements for packaging DNLEU
How to self-upload evidence when making an application to come to or stay in the UK.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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