Submit study materials as Microsoft Word documents whenever possible. Study materials include consent documents, recruitment materials, data collection instruments, etc.
iMedRIS includes an internal document comparison tool that helps the IRB to review document changes more efficiently, reducing the review turnaround time of your IRB submissions. Researchers can also utilize this tool prior to submitting document changes (whether in response to an IRB request for changes or a researcher’s amendment request) ensuring all desired changes have been made and reducing the likelihood of additional rounds of review.
Note: This comparison tool does not work with PDFs, so upload Word documents whenever possible.
|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|
|HIPAA Authorization Template Language
(If you research involves protected health information under HIPAA, insert the HIPAA authorization template language in your informed consent document.)
|Elements of Informed Consent||Revised 10/19/2018|
|Standard Informed Consent Template for Research||Word||Revised: 10/30/2018|
|Standard Parent Permission Template for Research||Word|
|Informed Consent for Anonymous Surveys||Word||Revised 10/30/2018|
|Sample Assent Form||Word|
|Informed Consent Template for Federally-Sponsored Research||Word||Revised: 10/30/2018|
|Informed Consent for Use of Non-Research Material||Word|
|Parent Permission for Use of Non-Research Material||Word|
|Assent for Use of Non-Research Material||Word|
|Parent Permission and Assent for Use of Non-Research Material||Word|