OHRP: What is Human Subjects Research?
This two-part session explains how to prepare a research proposal that addresses the regulatory requirements for review including the requirements for informed consent and helps investigators understand their responsibilities with respect to IRB review and protections of human research participants.
Part 1: A Review of the Common Rule and Its Application
Part 2: What Investigators Should Know About IRB Review
Recorded Session: 2021 NIH Virtual Seminar on Program Funding & Grants Administration