Routine fMRI Behavioral Component Informed Consent Template

Topic

Routine fMRI

Type

IRB-HSBS Website Directory and Guidance

(Word) General template to create an informed consent document for studies using the Routine fMRI Master Protocol to be reviewed by IRB-HSBS. Last Updated: 03/29/2019

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The University of Michigan has an approved Federalwide Assurance (FWA) with the U.S. Department of Health & Human Services (HHS). U-M’s IRBs are also registered with the HHS Office for Human Research Protections (OHRP).

U-M FWA Number: FWA00004969
U-M Institution/Organization Number: IORG0000144

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