Research & Development Website
Research in Progress
Progress Reports
- Guidance for Clinical Trials of Investigational Medicinal Products
- Guidance for all Other Research
- Funding Body Requirements
Guidance for Clinical Trials of Investigational Medicinal Products
All progress reports should be signed by the chief investigator (CI) and the CI may be requested to attend a meeting of the main REC or its sub-committee to discuss the progress of the research. Progress reports should only be sent to the main REC and copies should not be sent to other local RECs. Local principal investigators are not normally required to submit progress reports on the conduct of the research to the relevant local REC.
Please forward a copy of the COREC Clinical Trial of Investigational Medicinal Products Progress Report pro forma to the following:
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Main REC that provided a favourable opinion – REC contact details
- Competent Authority – MHRA
-
Research Sponsor – where LTHT/UoL is the sponsor, please send documentation to the R&D Department
- R&D Department - if the Trust or University is not the Sponsor, please send the report to the R&D Department
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Guidance for All Other Research
All progress reports should be signed by the chief investigator (CI) and the CI may be requested to attend a meeting of the main REC or its sub-committee to discuss the progress of the research. Progress reports should only be sent to the main REC and copies should not be sent to other local RECs. Local principal investigators are not normally required to submit progress reports on the conduct of the research to the relevant local REC.
Please
forward a copy of the COREC Other
Research Progress Report
pro forma to the following:
-
Main REC that provided a favourable opinion – REC contact details
-
Research Sponsor – where LTHT/UoL is the sponsor, please send documentation to the R&D Department
- R&D Department - if the Trust or University is not the Sponsor, please send the report to the R&D Department
Funding Body Requirements
The organisation providing funding for the study is also likely to require an annual update on the progress of the study. If the University of Leeds is administering the grant, you will be notified when this report is required.
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