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