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- HRA complaints policy and procedure
- Public involvement in a pandemic Q&A
- Praise for Research Ethics Committee members from Chief Medical Officer Chris Whitty
- Chief Executive, Teresa Allen, announces her retirement
- Genetic research and the HRA: celebrating the 20th anniversary of the Human Genome Project
- MHRA and HRA Position on who can act as a Chief Investigator
- Complex Innovative Trials: calls for new guideline adoption to get medicines to patients faster
- The Health Service (Control of Patient Information) Regulations 2002: regulation 5 decision procedure for research applications
- Non-Executive Directors appointed to HRA Board
- Combined ReviewCombined review
- Researchers are ‘missing a trick’ with public involvementHealth researchers are 'missing a trick' by not demonstrating how patients and the public have contributed to the design and conduct of research, the HRA has said.
- Confidentiality Advisory Group: understanding public views on using personal dataWhat are the circumstances under which it is acceptable to use confidential patient and service user information without consent for purposes beyond direct patient care?
- Research tissue banks and research databasesIf you are planning to create a research database or a research tissue bank (‘biobank’) then the following information may be helpful.
- Roles and responsibilitiesIt is important to ensure you have the right people in the correct roles supporting your project. When it comes to your project based research we would expect your research team to include the following roles, which is in line with policy and legislation; Sponsor; Sponsor’s legal representative; Chief Investigator; and Principal Investigator.
- Jonathan Fennelly-Barnwell appointed Interim Director of Approvals
- HRA Community Survey 2026
- Blog: Clinical trials regulations - six month countdown begins - 28 October 2025
- 5.3 Compliance with national legislation regarding Adults unable to consent to themselves in a non-CTIMP
- 2. Risk to participants
- Speed