" /> Data Monitoring Committee - CISMeF





Preferred Label : Data Monitoring Committee;

NCIt related terms : Data and Safety Monitoring Board; data monitoring committee (DMC); IDMC; Data Monitoring and Oversight Committee; DMC; Independent Data Monitoring Committee; Data and Safety Monitoring Committee DSMB; DMOC; DSMB; DSMC; Data Monitoring Committee/Data and Safety Monitoring Board (DMC/DSMB);

NCIt definition : A group of experts that periodically assess information from an ongoing clinical study, including participant's safety and trial effectiveness.;

Alternative definition : CDISC: A group of independent experts who are appointed to monitor the safety and scientific integrity of a research intervention, protect the confidentiality of participant data, and to make recommendations to the sponsor regarding the stopping of the trial for safety, efficacy, or for futility. (After clinicaltrials.gov; Committee for Medicinal Products for Human Use (CHMP), 2005, EMA; FDA Establishment and Operation of Clinical Trial Data Monitoring Committees. March 2006); CDISC-GLOSS: A group of independent experts who are appointed to monitor the safety and scientific integrity of a research intervention, protect the confidentiality of participant data, and to make recommendations to the sponsor regarding the stopping of the trial for safety, efficacy, or for futility. [After clinicaltrials.gov; Committee for Medicinal Products for Human Use (CHMP), 2005, EMA; FDA Establishment and Operation of Clinical Trial Data Monitoring Committees. March 2006]; NCI-GLOSS: An impartial group that oversees a clinical trial and reviews the results to see if they are acceptable. This group determines if the trial should be changed or closed.; MRCT-Ctr: An independent group of experts that reviews study data to make sure that patient safety is protected. (https://mrctcenter.org/glossaryterm/data-monitoring-committee-data-and-safety-monitoring);

Codes from synonyms : CDR0000522956; CDR0000044658;

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08/05/2025


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