Clinical Trial Reporting and Close-down
Clinical Trial Reporting and Close-down
We will work with you in managing all aspects of reporting and close-down:
- closedown of trial sites
- closedown of supporting departments
- database lock
- contribution to preparation of final report
- contribution to preparation of papers and other outputs for journals and conferences
- project close-down reports to funders, MHRA and research ethics committees
- End of trial declarations
- Trial Master File (TMF) archiving
- data archiving and preparation of data for sharing
- data anonymisation
- financial reconciliation
- dissemination of results to participants