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Guidelines for RiskBased Monitoring Version 3.0SCTO PLATFORMS | GUIDELINES FOR RISKBASED MONITORING2Publisher Swiss Clinical Trial Organisation (SCTO) Bern, Switzerland Authors Monitoring Platform
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Central data monitoring is a systematic process used to oversee and analyze data collected during research, ensuring data quality and compliance with regulatory standards.
Individuals or organizations conducting research, including sponsors, investigators, and clinical sites, are typically required to file central data monitoring.
To fill out central data monitoring, one must collect relevant data, complete the required forms accurately, and submit them to the designated regulatory body or monitoring authority.
The purpose of central data monitoring is to ensure data integrity, identify discrepancies, and facilitate compliance with ethical and regulatory guidelines throughout a study.
Information that must be reported includes data collection methods, participant information, compliance with protocols, results of quality checks, and any identified issues.
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