Budgeting for Single IRB Review
Single IRB (sIRB) review has become a standard requirement for many clinical trials: National Institutes of Health (NIH), Office for Human Research Protections (OHRP), and others now mandate centralized oversight for most multisite studies.
But not all research professionals are fully aware of these requirements, which can lead to operational and financial challenges.
Join this webinar for a practical discussion of external IRB reliance strategies, while accurately budgeting and planning for sIRB review. The University of Rochester will provide case study examples during the webinar.
Learning Objectives:
After attending this webinar, attendees will be able to:
- Describe what researchers and HRPP professionals should know about budgeting and planning for sIRB oversight
- Identify the sIRB options available for researchers
- Recognize ways institutions and IRB administrators can support sIRB requirement
Presented By
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Frank Conte
MS
Vice President, Institutional Partnerships
Advarra
Kelley O’Donoghue
MPH, CIP
Associate Vice President for Human Subject Protection
University of Rochester
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DATE: June 17, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour