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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
How to use a randomised controlled trial to evaluate your digital health product.
How to use a crossover randomised controlled trial to evaluate your digital health product.
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.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How investigators and sponsors should manage clinical trials during COVID-19
Actions that trial sponsors should consider to build resilience into clinical trial design
The MHRA is ready to provide any assistance for clinical trials applications submitted for COVID-19
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