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- Our people
- Feedback from the consultation
- SL-AR3
- Non-CTIMP Standard Conditions
- Updates to existing definitions
- I was a REC member for 38 years: an interview with Dr John Bull
- Guest blog: Some thoughts as I retire on why public involvement matters so much to the work of the HRA - by Jim Elliott, retired Public Involvement Specialist
- Clinical Trial Registration Audit Report
- Our full response to WHO consultation on improving clinical trials - 14 December 2022
- The Make it Public group
- Business plan 2021 - 2022
- Accountability report
- How the launch of Radiation Assurance is making an impactHow the launch of Radiation Assurance is making an impact
- Patient data and research leaflet
- Ending your projectThe definition of the end of the study should be documented in the protocol. In most cases, this will be the date of the last visit of the last participant or the completion of any follow-up monitoring and data collection described in the protocol.
- 6. Approvals and authorisations
- How being a REC member works alongside my career
- Blog: Information governance in research - an update on our work to improve assurances
- The approvals process for applications
- My first year as a REC member: an interview with Yinka Cole