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- HRA supporting new National Commission on the Regulation of AI in Healthcare
- Appendix C: Summary of Changes
- 5.5 Compliance with any other applicable laws or regulations
- Ease
- 9. Next steps
- 6. Contacting potential participants
- Be part of our advisory group on simplified arrangements for consent
- How we champion public involvement in researchDiscover how the Health Research Authority champions public involvement in health and social care research. Learn about our initiatives, partnerships and commitment to embedding patient and public voices and experiences in research design, delivery, and dissemination.
- Supporting the UK Standards for Public Involvement
- Our response to the government's update on its Lord O'Shaughnessy review progress
- The risk and control framework and the capacity to handle risk – long description
- How different perspectives and experiences have shaped our 2025-28 strategy
- Our aim and strategic objectives support UK government objectives
- How we work in partnership to make it easy to plan, support, manage and complete health and social care research in the UK
- We set shared expectations for how to do research and encourage compliance with these
- Anyone can understand what we do and why it matters to them and be confident in our decisions
- Automatic deferral scenarios for Phase 1 healthy volunteer trial applications - long description
- Deferrals in Phase 1 trials
- Target timeframes that RECs will work towards for modifications to Phase 1 healthy volunteer trials - long description
- How clinical trials of investigational medicinal product applications will be processed from 28 April 2026 - long description