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How to use a quasi-experimental study to evaluate your digital health product.
How to use an interrupted time series to evaluate your digital health product.
Using an ecological momentary assessment to evaluate your digital health product.
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information on how the CMA investigated the merger, and how you can find out more.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
How to use a crossover randomised controlled trial to evaluate your digital health product.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Getting a UK background check so you can apply for Global Entry and get through USA border control faster: how to apply, how much it costs
Bringing pets into Great Britain: pet passports, Great Britain pet health certificates, microchipping, rabies vaccinations, travelling with assistance dogs.
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Submissions related to human medicines need to be submitted directly to the MHRA.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to use an ethnographic study to evaluate your digital health product.
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