Institutional Review Board
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Table of Contents
Table of Contents
This course provides educational information and does not replace professional medical advice, diagnosis, treatment, or clinical judgment.
Transition from a researcher navigating ethics to a skilled IRB professional who safeguards participant rights and ensures regulatory compliance.
What You Will Learn
- 1 Understand the historical foundations and ethical principles underlying human subjects research.
- 2 Apply regulatory frameworks including the Common Rule, FDA regulations, and institutional policies.
- 3 Analyze the composition, functions, and operational procedures of an IRB.
- 4 Differentiate among exemption, expedited review, and full board review criteria.
- 5 Evaluate informed consent processes and protections for vulnerable populations.
- 6 Assess and categorize research risks and potential benefits.
- 7 Implement continuing review and post-approval monitoring procedures.
- 8 Communicate investigator responsibilities and required training components.
- 9 Manage IRB oversight for international and multi-site research projects.
- 10 Examine emerging ethical challenges in big data, artificial intelligence, and telemedicine research.
What's Included
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Institutional Review Board