How To:

- Meet IHMC's Human Research Participants training requirements

- Determine if your study involves Human Research Participants

- Set up your IRB account

- Submit a study protocol for review

- Renew a protocol (continuing review)

- Modify an existing protocol

- Close out an existing protocol

Useful Documents:

- HIPAA release form template

- IRB Certification form (required by some federal sponsors)

- Fillable log for protocol deviations

- IHMC's IRB Policies and Procedures

Current IRB Registration Forms:

- Federalwide Assurance (FWA)

- IRB Organization (IORG)

Single IRB (sIRB):

IHMC is a member of SMARTIRB, if collaborating with an external organization, check here to see if that organization is a member as well

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