All IRB applications must be submitted through iMedRIS.
Since the IRB review process is now accomplished online through iMedRIS, it is no longer necessary to print and fill out these forms. However, they can be useful resources for those who prefer to compile all necessary documentation prior to signing in to the IRB software.
|IRB Review Checklist||Posted: 3/2013|
|Categories for Exempted Review||Word|
|Categories of Research Qualifying for Expedited IRB Review||Word|
|Research Team Member’s Pledge of Confidentiality (Sample)||Word|
|Transcriber’s Pledge of Confidentiality (Sample)||Word|
|Researcher Pledge of Confidentiality to Protect SurveyMonkey Data||Word||Posted: 1/20/2012|
|HIPAA Authorization Template Language
(If you research involves protected health information under HIPAA, insert the HIPAA authorization template language in your informed consent document.)
|HIPAA Guidelines and Application Instructions||Word|
|Elements of Informed Consent|
|Sample Informed Consent Form||Word||Revised: 11/11/2015|
|Sample Consent Cover Statement||Word||Revised 11/11/2015|
|Sample Assent Form||Word|