Parkview Health

The Parkview Health IRB is compliant with all applicable federal and state laws and regulations governing IRBs and research with human subjects. PH IRB maintains written procedures for initial and continuing review of clinical trials, prepares written minutes of convened meetings, and retains records pertaining to the review and approval process. 

IRB forms are available for initial study submission and reporting other activities through the course of research studies.

1. 2012 PH IRB Meeting Dates
2. IRB Contact List
3. Amendments
4. Continuing Review
5. Deviation and Noncompliance Reporting
6. Electronic Submission and Review Process
7. Emergency Use of a Drug, Biologic, or Medical Device
8. Exempt Research List of Categories of Research
9. Exempt Research Protocols
10. Expedited Review-Categories of Research That May Be
       Reviewed by An IRB through an Expedited Review
11. Expedited Review of Research
12. Humanitarian Use Device (HUD)
13. IRB Introduction
14. IRB Authority, Membership, Board Positions
15. IRB Fee Schedule and Charging Policy
16. IRB Meetings
17. IRB Member Roster
18. IRB Operations
19. New Protocol Submission
20. Principal Investigator Statement of Principles
21. Presenters Format
22. Reportable Events
23. Reporting Procedure
24. Review of Medical Devices-SR vs NSR
25. Review of Research
26. Study Closure
27. Submission Flow Chart
28. Training Requirements for Individuals Involved in Human
       Subject Research
29. Use of a Centralized IRB
30. Use of a Centralized IRB − Approved List of Centralized IRBs
31. Vulnerable Populations