IRB Forms

• Addendum Checklist
• Addendum for Non-Inteventional Studies
• Adverse Event Form
• Continuing Review Form
• Exemption Request
• Expedited Review Request
• Investigator Checklist
• Termination Checklist
• Glossary of Terms

IRB Policies

• Adverse Event Reporting
• Emergency Use of Unapproved Medical Devices
• Fee Policy
• Humanitarian Use Device
• Informed Consent
• Off-Label Use
• Risks and Benefits
• Scientific Misconduct
• Special Populations Cognitively Impared
• Submission of New Protocol
• Termination of Protocols

 

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