Enhancing clinical research quality and safety through specialized nursing practice.
Day 2: November 18, 2022
8:30 AM — 9:30 AM: FDA - IND and IDE Process | Sean O'Connor (Director, IND Office, MD Anderson Cancer Center) | Patty Mendoza, MS, BA, BSN, RN, CCRC, CHRC, CCRP (Clinical Research Compliance and Regulatory Affairs Expert
9:30 AM — 10:30 AM: Informed Consent - Special Circumstances | Rosleen Mansour, MA (Senior Research Associate, UTHealth) | Raquel R Bunge, RN, BSN, CCRC, (Nurse Manager Quality Assurance, HMRI Academic Office of Clinical Trials, Houston Methodist Hospital)
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10:45 AM — 11:45 AM: Clinical Trial Registration | Elizabeth Gendel, PhD (Assistant Director, Research Compliance UTHealth
11:45 AM — 12:45 PM: Writing SOPs for Clinical Trial Sites | Linda C. Higgins, CCRP (Research Administrator, Uro-Research LLC)
For more information, visit: https://us02web.zoom.us/webinar/register/WN_dgE3xkdPTTSGznliN16Uig
International Association of Clinical Research Nurses
PO Box 7Mullica Hill, NJ 08062, USA(609) 519-9689 (Phone)firstname.lastname@example.org
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