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IRB Member Forms

Welcome to the IRB Members page. This page was created to provide materials to members of the Spectrum Health IRB.

  Version Date
Meeting Information  
IRB Contact Roster  09/09/2014
IRB Membership Roster 12/24/2014
Current IRB Roster 10/28/2016
 Checklists
Devices 02/15/2015
Drugs 02/15/2015
Eligibility for Review Using the Expedited Procedure 01/01/2015
Engagement Determination 05/05/2010
Exemption Determination 11/06/2009
Human Research Determination 08/27/2010
Non-Committee Review 08/27/2010
Non-Significant Risk Device 08/11/2010
Research Involving Children 08/11/2010
Research Involving Cognitively Impaired Adults 08/11/2010
Research Involving Neonates of Uncertain Viability 08/11/2010
Research Involving Non-Viable Neonates 11/05/2009
Research Involving Pregnant Women 08/11/2010
Research Involving Prisoners 08/11/2010
Waiver of the Consent Process for Planned Emergency Research 03/04/2010
Waiver of Written Documentation of the Consent Process 08/27/2010
Waiver or Alteration of HIPAA Authorization 06/14/2012
Waiver or Alteration of the Consent Process 03/04/2010
 Worksheets
Advertisements 11/05/2010
Contract Items Related to Human Subject Protections 11/23/2009
Criteria for Approval and Additional Considerations for HUD 08/16/2010
Criteria for Approval and Additional Considerations 05/10/2012
Department of Defense  05/10/2012
Emergency Use of a Test Article 12/25/2009
HIPAA Authorization for Research 11/14/2014
Scientific or Scholarly Review 11/05/2009
Payments 01/11/2012
Review of Information Items 02/10/2012
Short Form of Consent Documentation 11/05/2009
Other Resources  
Research Acronym Tool   
Writing A Review Summary
45 CFR 46: DHHS - Protection of Human Subjects   
FDA 21 CFR 50 Protection of Human Subjects   
FDA 21 CFR 56 Institutional Review Boards   
FDA Information Sheets: Guidance for IRBs and Clinical Investigators   
The Belmont Report   
Jesse's Intent