North Texas Chapter: Navigating the Single IRB Process (ACRP 2024 Conference Replay)
This event will be showing a ACRP 2024 conference replay.
Event Description:
Most federally funded, multisite studies already require oversight by a single institutional review board (sIRB), and soon that likely will be true for U.S. Food and Drug Administration-regulated studies. sIRB review presents challenges for study teams, especially those managing investigator-initiated studies. This program will navigate the challenges and responsibilities associated with the use of a single IRB.
Speakers:
Polly Goodman, Associate Director of Regulatory Affairs Operations, SMART IRB, Harvard Catalyst | The Harvard Clinical and Translational Science Center,
Michael Linke, PhD, Adjunct Professor/Director of Education, University of Cincinnati/SMART IRB
Event Agenda:
11:45 am - 12:00 pm CST – Log in
12:00 - 1:00 pm CST – Video & Q&A
Registration & Contact Hour Information:
- Chapter Member (registration with or without contact hours): $0
- ACRP Member (registration only): $0
- ACRP Member (registration + contact hours): $15
- Non-Member (registration only): $0
- Non-Member (registration + contact hours): $30
After registering, please visit the event's community page to find the login information or any additional event updates, and to communicate with the event organizer.
To claim contact hours: Purchase the contact hours and attend the program. After attending the event, log on to the ACRP website and visit learning.acrpnet.org, click “ACCESS ON DEMAND CONTENT”. Find the event in your dashboard, confirm attendance, and take the event evaluation between 1 and 30 days following the event and obtain the online certificate. After 30 days, contact hours are no longer available.