Centralized Review Process Markedly Expedites Approval of Cancer Clinical Trials
News Oct 20, 2009
This study of the CIRB was performed by scientists at the Veterans Affairs Palo Alto Health Care System (VAPAHCS) and Stanford University School of Medicine, Palo Alto, Calif., with assistance from NCI and appears online October 19, 2009 in the Journal of Clinical Oncology.
Over the past 40 years, more than 1,700 institutions in the United States have enrolled up to 20,000 patients annually in phase III clinical trials coordinated by NCI and have used separate IRBs to monitor research involving patients. Federal regulations require that most NIH-funded clinical trials be monitored by an IRB.
Drug Discovery Alliance Formed to Help Increase Drug Development Success RateNews
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First Ever Online Event Focused on Cannabis ScienceNews
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Autism Risk Higher if Pregnant Mothers Have Infection Requiring HospitalizationNews
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