Many AMRC members fund research in the NHS. To make sure that research involving patients is available and discoverable for patients, clinicians, and other stakeholders, it is important to register and report it. These pages provide guidance on what needs to be done across the timeline of clinical research to achieve this and the funder’s role in this space.
What is trial registration and where do people go for it?
What is required in results reporting?
How can charities support clinical research transparency?
Definitions
Sources