IRB - Application Requirements & Forms
All investigators planning on doing research at Synergy Medical, Covenant HealthCare and St. Mary's must complete the following tutorial and submit a copy of the certificate of completion to the Synergy Research Department with their IRB application.
Tutorial Link: http://phrp.nihtraining.com/users/login.php
IRB Application for all Projects:
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Word version |
Other Related Forms:
All applications submitted MUST have:
| 1. | Application signed by FACULTY principle investigator |
| 2. | CVs of ALL investigators listed on the project |
| 3. | Study protocol with SCIENTIFIC MERIT of study |
| 4. | Data collection tool / Survey |
| 5. | Consent Form if study involves human subjects If all of these are not included review will be DELAYED, which will subsequently delay the start of the project |
| 6. | Copy of certificate of completion from the human participant protections tutorial |
If you have question s about the application or the IRB in general, please contact John Clements at (989) 583-6861, jclements@synergymedical.org or Leslie Francke at (989) 583-6984, lfrancke@synergymedical.org.