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What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
Information about the EU Regulations and their implementation in Northern Ireland
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Check the tariff classification for dried buffalo ears and dried beef meat scraped off from the throat, for use as animal feed.
Use this form to file a translation in connection with a European patent or a European patent application
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
Form to report patients meeting the case definition.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
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.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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