Note:This training is offered online by CITI

CITI Course Name

IRB GCP for Social and Behavioral Research Best Practices in Clinical Research 
Required Modules
  1. Introduction
  2. Research Protocol
  3. Recruitment and Retention
  4. Informed Consent Communication
  5. Privacy and Confidentiality
  6. Participant Safety and Adverse Event Reporting
  7. Quality Control and Assurance
  8. Research Misconduct
  9. Conclusion
Passing Score Learners must take a short quiz at the end of each module. An average score of 80% is needed to pass the training.
IRB Prerequisite

Researchers working on a clinical trial must take a relevant Good Clinical Practice course, in additionto a foundational human subjects research course. 
Valid for  5 Years
Duration About 3 hours