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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.