- IRB Updates
- Does my project require IRB review?
- Submission Deadlines
- Procedures
- Forms
- Research Support System (RSS)
- Existing Paper Protocols
- Recruitment Templates
- Miscellaneous
- Subjects' Rights and Responsibilities
- Adult FWA Letter
- Peds FWA Letter
- Short Forms
- Which Application Do I Use?
- Exempt Studies
- Central IRB
- ClinicalTrials.gov
- Posting Consent Forms
| Title | Version | Format |
| 1. Appendix-Personnel Change Form | 08-17-10 | Word |
| 2. Investigator Assessment Checklist for Regulatory Documentation | 09-17-07 | Word |
| 3. Investigator Assessment of IRB | 09-17-07 | Word |
| 4. P&T Drug Registry Form | 04-14-22 | Word |
| 5. Assessment of Capacity to Consent to Participate in Research | 03-04-19 | Word |
- IRB Updates
- Does my project require IRB review?
- Submission Deadlines
- Procedures
- Forms
- Research Support System (RSS)
- Existing Paper Protocols
- Recruitment Templates
- Miscellaneous
- Subjects' Rights and Responsibilities
- Adult FWA Letter
- Peds FWA Letter
- Short Forms
- Which Application Do I Use?
- Exempt Studies
- Central IRB
- ClinicalTrials.gov
- Posting Consent Forms