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Information to support your recovery after COVID-19.
How to access the historical censuses from 1841 to 1921.
How to use a quasi-experimental study to evaluate your digital health product.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
Animal bites and pasteurella infections information for healthcare staff.
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out about your human rights and how they are protected.
Register your decision on the NHS Organ Donor Register. This will give your loved ones the certainty they need to support your choice.
Browse cases data for specific areas within the UK.
Blogs where government organisations talk about their work and share information and ideas.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
The official report of all Parliamentary debates. Find Members, their contributions, debates, petitions and divisions from published Hansard reports dating back over 200 years.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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