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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
How to use an N-of-1 study to evaluate your digital health product.
This Procurement Policy Note (PPN) updates the Selection Questionnaire (SQ) and accompanying statutory guidance and replaces PPN 03/23.
Customer declaration of specific uses of the scheduled category 1 or 2 substances (individual transactions).
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
Export controls on goods that can be used for torture or capital punishment.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
How investigators and sponsors should manage clinical trials during COVID-19
Employment Appeal Tribunal Judgment of Mr Justice Kerr on 23 May 2024.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
How to use a single commodity code to import your goods in split consignments when importing large machinery or plant.
Working with others to embed the importance of place within the published guidance.
Find out if your university qualification means you're eligible for a High Potential Individual visa.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Submissions related to human medicines need to be submitted directly to the MHRA.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
You must apply to register with Ofsted if you are the registered person, a registered individual or the nominated individual of a daycare.
Guidance for manufacturers, importers and distributors.
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