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If you are looking for research summaries please go to the research summary page.
- Approvals and amendmentsThe Health Research Authority provides approvals and opinions for research studies. This section will help you understand what services you require and how to navigate and manage your application.
- What approvals and decisions do I need?One of the first steps in deciding which approvals you need for your project is to determine whether it is classed as research, and therefore whether it should be managed as such. The responsibility for determining whether a project is classed as research lies with the managing organisation. For studies that are determined to be research, the managing organisation would then accept the role of sponsor.
- 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.
- Gaining HRA approval - long description
- UK study-wide governance criteria
- 1. Application package
- 2. Risk to participants
- 3. Risk to study
- 4. Risk to organisation
- 5. Legal compliance
- 5.1 Assessment of Information Governance, Data Protection Compliance and Data Security
- 5.2 CTIMPS - Arrangements for compliance with the Clinical Trials Regulations assessed
- 5.3 Compliance with national legislation regarding Adults unable to consent to themselves in a non-CTIMP
- 5.4 Compliance with national legislation regarding Human Tissue
- 5.5 Compliance with any other applicable laws or regulations
- 6. Approvals and authorisations
- Appendix A: Areas of review in HRA assessment which are additional to the UK study wide governance criteria
- Appendix B: Footnotes
- Appendix C: Summary of Changes
- Research Ethics Committee reviewResearch Ethics Committees (RECs) review research applications and give an opinion about whether the research is ethical. They look at areas such as the proposed participant involvement and are entirely independent of research sponsors (that is, the organisations which are responsible for the management and conduct of the research), funders and investigators. This enables them to put participants at the centre of their review.