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The top documents tagged [irb approval]
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irb approval
FLYING SAMS AT UCSD WINTER WEEK 3 GBM Jan 23 2013 .
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Understanding Research: Getting Your Project Ready for the IRB Jill Stoltzfus, Ph.D. Director, Research Institute
[email protected]
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218 views
FDA Regulation of Pharmaceuticals and Devices Jean Toth-Allen, Ph.D. Good Clinical Practice Program Office of Science and Health Coordination Office of.
212 views
Regulation of Medical Devices Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation.
216 views
What is HIPAA ? HIPAA with the DHPG Research Medical Records Clinical Trials Business Associate Agreement Michael Shoob, Elizabeth BankertFebruary 2003.
215 views
USC Clinical Trials Office (CTO) Submitting your Studies to CTO For Processing Soheil Jadali Director, Clinical Trial Office.
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Introduction to Research Pharmacy Investigational Drug Control and Patient Safety CUMC RP Robert B. MacArthur, Pharm.D.
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Is it Research?. Is It Research? 2 Elements –The project involves a systematic investigation –The design (meaning goal, purpose, or intent) of the investigation.
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Food and Drug Administration Center for Biologics Evaluation and Research The Office of Cellular, Tissue, and Gene Therapies Web Seminar Series presents:
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Pilot Studies Nuts and Bolts Deborah Grady, MD, MPH Professor of Medicine Associate Dean for Clinical and Translational Research UCSF.
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Maximizing Public Data Sources for Sequencing and GWAS Studies
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Or rab update 050510final
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