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Discover the standard operating procedures for clinical trial registration and maintenance in the CORP to ensure compliance and data accuracy for NCI-designated cancer centers.
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The clinical trial reporting program is a system established to collect and disseminate data on clinical trials to ensure transparency and accountability in medical research.
Investigators, sponsors, and organizations conducting clinical trials are required to file reports with the clinical trial reporting program.
To fill out the clinical trial reporting program, participants should complete the required forms detailing the trial's design, results, and other relevant information.
The purpose of the clinical trial reporting program is to promote transparency, facilitate access to evidence for healthcare decisions, and enhance public trust in the research process.
Information that must be reported includes trial registration details, study design, participant demographics, outcome measures, and results of the trial.
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