Search results
If you are looking for research summaries please go to the research summary page.
934 results for at
- Use of human tissue in researchThis section relates to the application of the Human Tissue Act 2004 to issues of consent, ethical review and licensing.
- Mental Capacity ActThe Mental Capacity Act 2005 (MCA) provides a comprehensive framework for decision making on behalf of adults aged 16 and over who are unable to make decisions for themselves, i.e. they lack capacity.
- Publishing your research findingsThe results of research should be reported, whether through publication in peer reviewed journals or other means of dissemination. Negative as well as positive results should be published, or at least made publicly available.
- VacanciesThe HRA is a dynamic organisation, delivering excellent services through its committees, simplifying the health research process and championing research in the NHS. We hope that you are as enthused by our vision, our plans and our operations as we are.
- Radiation AssuranceRadiation Assurance is a UK-wide process fully managed by the HRA on behalf of all four UK nations.
- Guidance and policy for REC membersGovernance Arrangements for Research Ethics Committees (GAfREC): a harmonised edition (DH, 2011) outlines the policy of the UK Health Departments, describing what is expected from the research ethics committees that review research proposals relating to areas of the departments’ responsibility.
- HRA ApprovalHRA Approval is for all project-based research that involves NHS organisations in England where the NHS organisation has a duty of care to participants, either as patients/service users or NHS staff/volunteers. References to participants include people whose data or tissue is involved in a research project.
- Who we are
- Blog: turning feedback into action: what we’ve achieved this year
- How non-CTIMP applications will be processed from 28 April 2026 - long description
- Christmas opening hours 2025
- Share your feedback on planned changes to the model Clinical Trial Agreement (mCTA)
- World Health Organization launches Global Clinical Trials Forum
- Blog: Why user research is essential to the success of our new digital services
- Final guidance to accompany updated clinical trials regulations is published - 1 October 2025
- 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