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- Research Transparency Annual Report 2021
- Clinical trial registration audits
- Clinical trial registration report 2022
- Transparency roadmap
- Clinical Trial Registration Audit Report
- Research Transparency Annual Report 2022/23
- Clinical Trial Registration Audit Report
- Make it Public week 2024
- Parklife: a poem for Make it Public week 2024
- Make it Public workshop summary
- Good Clinical PracticeGood Clinical Practice (GCP) is a set of internationally recognised ethical and scientific quality requirements that must be followed when designing, conducting, recording and reporting clinical trials that involve people.
- Joint Statement on the Application of Good Clinical Practice to Training for Researchers (HRA, MHRA, Devolved Administrations for Northern Ireland, Scotland and Wales)
- Clinical Trials of Investigational Medicinal ProductsLegislation sets out how drug trials are approved, conducted, monitored and reported.
- Combined reviewcwow amendment
- How the combined ways of working pilot is already making an impact
- Technical Assurance submission guidelines for combined review applicants
- Step by step guide to using IRAS for combined review
- A screen shot of CWoW IRAS which reads
- A screen shot showing a section of CWoW IRAS which reads:
- CWoW IRAS screen shot about selecting sponsor group