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Description
The difference between activities that meet the definition of “research” and those that do not can be hard to discern. Drawing from her 30+ years of experience the presenter shares a clear framework that will help you distinguish quality improvement (QI) activities from regulated research activities. During the webinar, we explore the characteristics of QI activities and the potential overlap of QI and regulated research. Considerations for when IRB review is required and case studies conclude the webinar.
Note: This advanced webinar is for learners who already have foundational knowledge of the Common Rule (45 CFR 46, Subpart A) and regulatory definitions.
Audience
IRB Administrators, IRB Directors, IRB Members, Researchers
Meet the Presenter
Linda Reuter, MS, CIP – Biomedical Research Alliance of New York (BRANY)
Linda is the IRB Director at BRANY. She holds a BS in Biology and MS in Health Science. Over a 30 year career Linda has traveled the country providing IRB training/education, audit services, and general consulting to numerous IRB programs. She has also contributed to various publications in her field.
