IRB Forms & Templates
Review and Approval Process
The Metro Health Institutional Review Board (IRB) is charged with protecting the rights and welfare of participants in clinical trials and other human subjects research studies conducted at Metro Health. They are responsible for monitoring compliance with federal and state laws, hospital policies and ethical principles outlined in the Belmont Report.
The following forms and templates are designed to assist the IRB with their review. If you have questions or are having trouble with any of the documents listed, please contact Jennifer Rice at (616) 252-5026.
Pre-Submission Tools & Templates
IRB Submission Forms
Contact Information Form 2/2012
Application for Human Research Form 7/2012
Modification of Approved Human Research Form 4/2012
Continuing Review Progress Report or Notification of Study Completion Form 4/2012
Reportable New Information 2/2014
**ANNOUNCEMENT: The HRPP/IRB will be transitioning to an electronic submission system in the Fall of 2018. Stay tuned for more information!**
Humanitarian Use Device (HUD) Forms
Decision Making Tools
The U.S. Department of Health & Human Services (DHHS) provides “Human Subject Regulations Decision Charts” to help researchers determine the proper level of review needed for their proposal. The table below lists the 11 different decision charts with a link directly to each one. If you need further guidance, please contact the IRB at mailto:email@example.com or 616-252-5026.
Question that is addressed Chart Research Activity Is your activity considered research Chart 1 Research Exemptions to IRB Review Is your human subjects research eligible for an exempt review by the IRB? Chart 2, Exempt If yes, what exemption category applies to your project? Chart 3, Educational Setting Exemption Chart 4, Tests, Surveys, Interviews, Public Behavior Observation Exemption Chart 5, Existing Data, Documents, Records and Specimens Exemption Chart 6, Public Benefit or Service Programs Exemption Chart 7, Food Taste and Acceptance Studies Exemption Expedited Review by the IRB If no exemption applies, is your human subjects research eligible for an expedited review by the IRB? Chart 8, Expedited Review If your application is related to a continuing research, is that one eligible for an expedited review by the IRB? Chart 9, Expedited Continuing Review Informed Consent Can informed consent be waived or consent elements be altered? Chart 10, Waiving/Altering of informed consent Can documents of informed consent be waived? Chart 11, Waiving of documentation of informed consent