Speaker: Maria Arnold, CIP, IRB Clinical Research Manager, Baptist Health South Florida Institutional Review Board
Target Audience: Physicians, Nurses, Research Administrators, Research Coordinators, Research Assistants, Performance Improvement
Presented On: March 10, 2016
Do you know what factors determine which studies are considered research and require IRB review and which studies do not? Do you know under what circumstances you need IRB acknowledgement versus IRB approval?
Learn how to follow the proper protocol for IRB submissions and differentiate when to utilize preparatory to research, exempt review, expedited review, full review, none of the above, and more.
Presenter: Maria Arnold, CIP
Clinical Research Manager
Baptist Health South Florida
Institutional Review Board
- Introduce the Office for Human Research Protection (OHRP) Notice of Proposed Rulemaking (NPRM).
- Help us understand how the NPRM will affect IRB review.
- Educate the research community on how the NPRM will affect IRB submissions.
- Provide guidance to ensure researchers comply with the NPRM.