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OHRP/FDA Guidance for Minutes of IRB Meetings

This guidance is intended to assist institutions and IRBs responsible for preparing and maintaining minutes of IRB meetings (also referred to in this guidance as minutes). This guidance document describes requirements for minutes and provides recommendations for meeting the regulatory requirements for minutes.

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*You must pass each module to progress through this course.

Lauren McReynolds - 1.5 CEUs
lmcreynolds@ecog-acrin.org

Modules in the Course:
OHRP/FDA Guidance for Minutes of IRB Meetings