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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.
Blogs where government organisations talk about their work and share information and ideas.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Pharmacovigilance system requirements
Letters issued to general further education colleges, sixth-form colleges and higher education institutions with a notice to improve.
Special feature articles on energy issues in the United Kingdom from the quarterly statistical bulletin Energy Trends.
Guidance for those affected by changes to UK immigration and borders due to coronavirus.
This amended guidance was issued under s 182 of the Licensing Act 2003.
Research into a range of gender and equality issues, including body image, gender norms, pornography use, shared childcare, and shared parental leave and pay.
How investigators and sponsors should manage clinical trials during COVID-19
This series brings together all documents relating to Research news
FCDO travel advice for Ecuador. Includes safety and security, insurance, entry requirements and legal differences.
The government's response to a report published by the House of Lords Select Committee on Risk Assessment and Risk Planning.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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.
Volume 52 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Find information and support on woodland creation in England, including funding to create woodland, legal requirements and best practice for sustainability.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Researchers around the world will soon be able to access millions of the natural, historic specimens found in UK museums at the click of a button as part of a £473 million UK fund to enhance key research infrastructure.
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