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Abstract Introduction: The Good Clinical Practice guideline identifies that data monitoring is an essential research activity. However, limited evidence exists on how to perform monitoring including the amount or frequency that is needed to ensure data quality. This study aims to explore the monitoring procedures that are implemented to ensure data quality in Australian clinical research studies. Material and methods: Clinical studies listed on the Australian and New Zealand Clinical Trials Registry were invited to participate in a national cross-sectional, mixed-mode, multi-contact (postal letter and e-mail) web-based survey. Information was gathered about the types of data quality monitoring procedures being implemented. Results: Of the 3689 clinical studies contacted, 589 (16.0%) responded, of which 441 (77.4%) completed the survey. Over half (55%) of the studies applied source data verification (SDV) compared to risk-based targeted and triggered monitoring (10–11%). Conducting

New zealandGood clinical practiceNew zealand clinical trials registryCentralized monitoringClinical trialData qualityRemote monitoringRisk based monitoringSource data verificationபுதியது ஜீலாந்துநல்ல மருத்துவ ப்ர்யாக்டீஸ்புதியது ஜீலாந்து மருத்துவ சோதனைகள் பதிவுமையப்படுத்தப்பட்ட கண்காணிப்பு