By participating in this continuing education program, the attendee should be able to:
- Describe the framework for IRB review
- Identify 3 criteria an IRB must consider when determining if a study is approvable
- Explain considerations that an IRB makes when evaluating risk/benefit ratio, minimization of risks and the composition of the informed consent document.
The faculty has no commercial relationships with any entity producing, marketing, reselling, or distributing health care goods or services consumed by, or used on, patients.