Module 1
- Overview
- Introduction
- Process
- Basic Principles
- Brief History
- What Research Must be Reviewed
- IRB Review Criteria
Module 2
- Overview
- Introduction
- Selecting Participants
- Describing Research
- Discussing Participation
- Ensuring Readability
- Assessing Understanding
Module 3
- Overview
- Continuing Review
- Unanticipated
Developments
- Adverse Events
- Consent Doc. Revisions
Module 4
- Student Test
- Faculty/Staff Test
Helpful Links
- NIH Protecting Human
Participants
- Office for Protection


JMU OSP

Module 2
The Consent Process

After completion of this module, you should be able to:

Continue to Introduction -->

<-- Return to IRB Review Criteria

 

 

Useful Links:
-SPA Accounting
-Research & Public Service
-Academic Affairs
-Office of Technology
Transfer

Last Modified July 3, 2008

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