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If you are looking for research summaries please go to the research summary page.
- Can I become a HRA-registered radiation reviewer?
- HRA Clinical Radiation Expert reviewer role description
- HRA Medical Physics Expert reviewer role description
- Radiation Assurance FAQs
- Radiation Assurance consistency review timelines graph long description
- Radiation Assurance total review timelines graph long description
- Technical Assurance review fee
- Technical Assurance Payments Framework Guidance
- Amending an approvalAmendments are changes made to a research project after approval from a review body has been given. Find out whether you need to notify the review bodies from whom you have received approvals.
- Examples of substantial and non-substantial amendmentsFind examples of substantial and non-substantial amendments.
- Template email for sponsors to confirm implementation of an amendment
- Template email for sponsors to share category C amendment documents with sites
- Template email for sponsors to share category A or B amendment documents with sites (regulatory approvals outstanding)
- Category A or B amendment documents with sites – where regulatory approvals in place
- Managing your approvalThis section covers what you will need to consider whilst you are conducting your research including progress reports, as well what to do at the end of your research.
- Progress reportsDepending on what approval you have received you will be asked to complete a progress report to keep us up to date with how your research is progressing.
- Safety reportingThe procedures for safety reporting will vary depending on your type of study.
- Safety and progress reports (other research) procedural table
- Safety and progress reports (CTIMPs) procedural table
- 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.