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 |