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How to use a quasi-experimental study to evaluate your digital health product.
Evidence considered by the Scientific Advisory Group for Emergencies (SAGE).
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Guidance on the Animal and Plant Health Agency laboratory testing services and prices for animal disease diagnosis.
A range of tests are available from the majority of PHE regional clinical microbiology laboratories.
How to apply for a fisheries dispensation from UK laws to carry out scientific research from a fishing vessel in English waters.
Technical advice and guidance for licence holders.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Events Research Programme (ERP) is building evidence on the risks associated with COVID-19 transmission routes, the characteristics of events and surrounding activities, and mitigation measures that can effectively address these risks.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
We carry out and commission research on a wide range of subjects which have implications for government policy.
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