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2018 Exploratory Workshop

Meeting New Challenges in Informed Consent in Clinical Research

FRIDAY, SEPTEMBER 7, 2018

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Session Summary

Session A: Welcome address & Laying the groundwork for meaningful informed consent

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Session B: Effectively presenting information to facilitate high-quality decision-making

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Session C: Pragmatic clinical trials (PCT) - challenges and innovations in getting informed consent

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Session D: Delivery room research and the challenges for informed consent & Moderators panel

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CIP Accreditation:

The 2018 OHRP Exploratory Workshop Meeting New Challenges in Informed Consent in Clinical Research meets the criteria in the Certified IRB Professional (CIP) recertification guidelines exit disclaimer icon and are eligible for accredited continuing education units. A maximum of 7.25 hours of continuing education credits can be claimed, proportioned as follows by session: A, 2 hours; B, 2 hours; C, 1.5 hours; D (with Moderators Panel), 1.75 hours.

Content created by Office for Human Research Protections (OHRP)
Content last reviewed September 6, 2024
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