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Considerations When Transferring Oversight to Another IRB

Please read this draft FDA Guidance which discusses the regulatory responsibilities of IRBs, clinical investigators, and sponsors when oversight of a previously approved clinical investigation under FDA's jurisdiction is transferred from one IRB to another IRB.

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

Erin Hyde- CEU 0.5
ehyde@ecogchair.org

Modules in the Course:
Considerations When Transferring Oversight to Another IRB