Adverse Event or Unanticipated Problem Form
Application Humanitarian Use Device Form
Continuation Form
Determination Form
Emergency Use Consent Form
Emergency Use Report
Enrollment Closure Form
Fee Schedule
Final Study Closure Application
Informed Consent Checklist
Initial Review Application
Modification Request Form
Protocol Closure or Suspension Form
Protocol Deviation Report Form
Request for Exemption
Request to ReOpen a Closed Study
Additional Research Personnel
Financial Conflict of Interest Disclosure Form
Multiple Adverse Events Reporting Form
Request for Approval of Deception in Research
Request for Waiver of Consent
Request for Waiver of Written Consent
Research Involving Cognitively Impaired Individuals
Research Involving Stored Data for Future Use
Use of Internet in Human Participants Research
Waiver of HIPPA Authorization
Adverse Event and Unanticipated Problems Reporting Policy
Allegations of Non-Compliance, Concerns or Complaints
Closure of Studies
Continuing Review 8.2019
Continuing Review
Emergency Use of Drugs, Biologics, and Devices
Exempt Review
Expedited Review
Expiration of IRB Approval and Subsequent Notice to Cease Study Activity
Financial Conflict of Interest
Human Subjects Research Policy
Humanitarian Use Devices
Informed Consent
Initial Review and Primary Reviewer System
Jurisdiction Authority
Membership
Non-English Speaking Subjects
Payment to Subjects
Planned Emergency Research
Record Keeping
Research Involving Children
Research Revision
Use of Non-Local IRBs
Voting
