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 Maureen Oostendorp 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
Humanitarian Use Device (HUD) Forms