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CTSA Institution

University of California, San Francisco

Disclaimer Please cite the appropriate authors/contacts when using or adapting these materials.
Acknowledgment Bernard Lo, M.D.
Professor of Medicine
Director, Program in Medical Ethics
Contacts Bernard Lo, M.D.
Format Links
URL http://www.ctspedia.org/do/view/ResearchEthics/DataMonitoring
Materials Provided Article
Title Data Monitoring in Clinical Trials
Topics Description An overview with valuable links of what is a Data Safety Monitoring Plan and when an investigator needs to have one. This depends on the type of clinical trial research proposed.
Keywords Blinded; Clinical Trials; Data Safety Monitoring Board (DSMB); Data Safety Monitoring Plan (DSMP); Informed Consent; Institution Review Board (IRB); Investigator; National Cancer Institute (NCI); National Institutes of Health (NIH); Participants; Protocol; Risk-Benefits; Study Sponsor; Unblinding
See Also

Topic Human Subjects, Other
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Topic revision: r6 - 05 Apr 2010 - 14:19:35 - MaryBanach
ResearchEthics.Data_Monitoring_In_Clinical_Trials moved from ResearchEthics.DataMonitoringInClinicalTrials on 06 Jul 2009 - 18:41 by CTSpediaAdmin - put it back
 
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