PresentsSusan Partridge, B.S.N., M.B.A., C.C.R.C.
Associate Professor of Pediatrics
Chief Operating Officer & VP Research Administration
L.A. Biomedical Research Institute at Harbor-UCLA Medical Center
FDA Regulations and Good Clinical Practices
Thursday, May 5, 2011
9am Hawaii, 12pm PDT, 1pm MDT, 2pm CDT, 3pm EDT, 3pm Puerto Rico
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Essential Documents for Clinical Trials
Wednesday, May 11, 2011
9am Hawaii, 12pm PDT, 1pm MDT, 2pm CDT, 3pm EDT, 3pm Puerto Rico
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Data Collection Standards for Clinical Trials
Wednesday, May 25, 2011
9am Hawaii, 12pm PDT, 1pm MDT, 2pm CDT, 3pm EDT, 3pm Puerto Rico
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Roger J. Lewis, M.D., Ph.D.
Professor of Medicine
Principal Investigator
Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center
Data Safety Monitoring (SMB/DSMP)
Wednesday, June 15, 2011
9am Hawaii, 12pm PDT, 1pm MDT, 2pm CDT, 3pm EDT, 3pm Puerto Rico
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Junko Nishitani, Ph.D.
Assistant Professor
IRB Director
Charles Drew University
Institutional Review Board (IRB)
Wednesday, June 8, 2011
9am Hawaii, 12pm PDT, 1pm MDT, 2pm CDT, 3pm EDT, 3pm Puerto Rico
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Informed Consent
Wednesday, June 22, 2011
9am Hawaii, 12pm PDT, 1pm MDT, 2pm CDT, 3pm EDT, 3pm Puerto Rico
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