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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Submission dates and how the submissions using the EC decision reliance procedure work.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
Browse cases data for specific areas within the UK.
Sign up for upcoming webinars to learn more about UK transition.
Learn about about importing and exporting goods.
Special feature articles on energy issues in the United Kingdom from the quarterly statistical bulletin Energy Trends.
This amended guidance was issued under s 182 of the Licensing Act 2003.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Blogs where government organisations talk about their work and share information and ideas.
Use form C&E48 to apply for authorisation to use simplified procedures for importing and exporting.
Pharmacovigilance system requirements
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
How investigators and sponsors should manage clinical trials during COVID-19
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