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IRB applications, forms and templates

These forms and tools are provided to assist organizations and study teams that rely on the Geisinger Institutional Review Board (IRB) as the IRB of record.

A specific form may be recommended or required as a supplement to the IRB's electronic applications, while other materials may be a useful reference when partnering with the Geisinger IRB in the protection of human research participants.

iRIS (IRB electronic system)

Protocol Development

Informed Consent