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May'04 Conduct of Clinical Research Workshop Materials |
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University of Florida's General Clinical Research Center
and the
Institutional Review Board
present: |
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ENHANCING THE CONDUCT OF CLINICAL RESEARCH AT THE UNIVERSITY OF FLORIDA |
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A Program for
Principal investigators, Researchers, Study
Coordinators,
Research Nurses and Staff |
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Workshop schedule (May 13-14, 2004) |
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Participants can click here to download presentations
and workshop materials.
(Materials will be available within two weeks of workshop.) |
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Thursday, May 13, HPNP Auditorium |
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8 - 9 a.m. |
Ethical and Legal Aspects |
Bill Allen, JD |
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9 - 10 a.m. |
Navigating Regulatory Committees |
Peter Iafrate, PharmD |
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10 - 10:15 a.m. |
Break sponsored by GCRC |
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10:15 - 11:15 a.m. |
Informed Consent |
Pam Schreck, MSN |
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11:15 - 12:15 |
HIPAA |
Susan Blair, MSJ, MBA |
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12:15 - 1:15 p.m. |
Lunch on your own |
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1:15 - 2:15 p.m. |
Good Clinical Practice |
Teresa d'Angelo, BSN, CCRC |
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2:15 - 3:15 p.m. |
Data Management - Best Practices |
Doug Theriaque,MS |
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3:15 - 3:30 p.m. |
Break sponsored by IRB |
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3:30 - 4:30 p.m. |
Reporting adverse events |
Michael Mahoney, BS |
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Friday, May 14, Room 210 HPNP Building -- IRB Track |
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9 - 10 a.m |
IRB Requirements for Informed Consent |
Linda Fallon, BSFRC |
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10 - 11 a.m. |
How to get a UF IRB approval |
Ken Kepler, MSSE |
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11 - 12:15 |
Lunch on your own |
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12:15 - 1:15 p.m. |
Recruiting Basics |
Michael Scian, MBA,JD |
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1:15 - 2:15 p.m. |
Medical Record Research |
Michael Mahoney,BS |
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Friday, May 14, Room 201 HPNP Building -- GCRC Track |
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9 - 10 a.m |
Laboratory Basics |
Allyson Fox, MSN |
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10 - 11 a.m. |
Monitoring - Data and Safety and QA Auditing |
Kris Wynne, BSN
Barbara Frentzen, MSN |
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11 - 12:15 |
Lunch on your own |
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12:15 - 1:15 p.m. |
Special Topics Panel - Research with Children |
Des Schatz, MD
Susan Horky, MS, LCSW
Sherri Mizrahy, MSN |
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1:15 - 2:15 p.m. |
Conflict of Interest |
M. Peter Pevonka, RPh |
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