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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.
Legal requirement for the sale of veterinary medicines on the internet and the VMD Accredited Internet Retailer Scheme (AIRS).
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Information about the EU Regulations and their implementation in Northern Ireland
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Make sure that domains that do not send email cannot be used for spoofing.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
Use this form to file a translation in connection with a European patent or a European patent application
Form to report patients meeting the case definition.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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
How to use A/B testing to evaluate your digital health product.
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