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IRRB Procedures

Pathway to IRRB Review
Description of the IRRB Process from start to finish

Protocol Requirements
Document outlining minimum requirements for protocols submitted for IRRB review.

SOP for Submission of New Human Subjects’ Research Studies
Procedural guide for completing a new research submission involving human subjects at Akron General Medical Center

Conflicts of Interest Disclosure Procedure
Description of Conflicts of Interest and how to manage a Conflict

SOP for Obtaining Informed Consent
Guidelines for Obtaining Informed Consent at AGMC

SOP for Amendment Requests
Procedural guide for completing a request for an amendment of a research study

SOP for Continuing Review of Research Studies
Procedural guide for completing the annual continuing review of research studies

SOP for Unanticipated Adverse Events
Description of Adverse Events and details of when to submit to the IRRB

Date Updated: 21-MAR-2017

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