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Register to vote Register by 18 June to vote in the General Election on 4 July.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Legal rules for trustees when deciding whether to accept, refuse or return a donation.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
If you manage an online platform that allows user generated content, these 7 steps will help you keep your business and your users safe.
Information about what Safety Recommendations are and how we make them as part of our investigations.
How to use a randomised controlled trial to evaluate your digital health product.
Use a Department for Education (DfE) approved framework agreement to help you buy goods and services for your school.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to use a cost utility analysis to evaluate your digital health product.
Why it's important to evaluate digital health products that have been developed rapidly and how to choose evaluation methods in these circumstances.
The RPC and Better Regulation Executive (BRE) have compiled a collection of links that may be useful for departments to use when writing impact assessments.
Guidance about working in collaboration with other charities.
Advice to ship owners for adopting the revised performance standards for shipborne voyage data recorders (VDRs) and simplified voyage data recorders (S-VDRs).
Information on the status of mpox as a high consequence infectious disease (HCID).
Emerging techniques on how to prevent or minimise the environmental impacts of post-combustion carbon dioxide capture.
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to use a quasi-experimental study to evaluate your digital health product.
Submissions related to human medicines need to be submitted directly to the MHRA.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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