12 Quality Assurances

IRB Policy 12.1 Educational Activities for IRB Reviewers (see archive)

IRB Policy 12.2 IRB Monitoring or Audits (see archive)

IRB Policy 12.3 Food and Drug Administration Monitoring or Reviews of the IRB– Information for the Reviewer and the Investigator (see archive)

IRB Policy 12.4 Non-compliance with Human Research Protection Program Requirements (see archive)

IRB Policy 12.5 Reports of Potential Non-compliance

IRB Policy 12.6 Findings of Non-compliance under IRB Policy 12.5