Institutional Review Board Policies
- Clinical Research Proposal Submission
- Promoting Objectivity in Research (Financial Conflict of Interest)
- Review Process for New Submissions
- Criteria for Approval
- Waiver of IRB Jurisdiction
- Investigator Responsibilities
- Informed Consent
- Waiver or Alteration of Informed Consent
- Surrogate Informed Consent
- Consent under Emergent Conditions
- Emergency Use of a Research Intervention
- Treatment Use of an Investigational Drug
- Humanitarian Use Devices
- Continuing Review
- Changes to Previously Approved Research
- Study Status
- Expedited Reporting of Serious Adverse Experiences and Unanticipated Problems
- Recruitment of Subjects
- Payment to Subjects
- Conflict of Interest
- Managing Allegations of Non-Compliance
- Uses and Disclosures of Protected health Information
- Privacy Board