Upon completion of the activity, participants should be able to:

1. Compare and contrast the current OHRP/FDA regulated IRB review process with an ethical perspective, exploring questions relating to the appropriate sphere of IRB oversight.

2. Identify where opportunities for IRB process improvement might lie.

3. Evaluate foundational human subjects' protection procedures in order to understand how to fulfill a human protections program's mission.

4. Develop strategies to successfully integrate psychological and group dynamics of IRB meetings.

5. Recognize optimal strategies for minimizing coercion and undue influence in subject recruitment methods.

6. Navigate the implementation of an electronic IRB system.

7. Recognize “mission creep” with respect to a human subjects' protection program.

8. Demonstrate mastery of concepts of human subjects' protection completing the CITI exam.

9. Evaluate the current and advancing ethical principles of human subjects' protections in relation to genetics research.

 

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A detailed schedule of presenters and speakers is here. [More]

At the end of the program, participants should be able to meet these objectives. [More]