Kuali IRB Policy Session: What Needs Review (Medical Research)
From Elaine Fleming
We’ve been making more use of flexibility in the regulations and adopting more industry best practices to better tailor our reviews to risk.
This webinar will cover:
- How we’re re-calibrating the jurisdiction of Human Research Protections Program (HRPP) and the IRB
- How you can anticipate what type of review you’ll need for different types of projects (or that you won’t need a review)
- What’s involved in the different types of review, including certain clinical activities that require IRB review such as humanitarian use devices or expanded access to investigational drugs for treatment
- How Kuali IRB is designed to lead you through, based on your project's requirements