At the end of the trial
After the last patient has completed per protocol follow-up we will work with you to ensure:
- All data cleaning is complete and the final data set is locked for analysis
- Closure of all participating NHS study sites
- Close of out any third-party suppliers
- Final reports submitted as appropriate to the study e.g. REC, MHRA, funders, stakeholders, participants, and to trial registries where appropriate.
- Ensure that the Trial Master File is locked and archived as required by the sponsor and applicable regulations.

