Meeting New Challenges in Informed Consent in Clinical Research
FRIDAY, SEPTEMBER 7, 2018
Session A: Welcome address & Laying the groundwork for meaningful informed consent
Session B: Effectively presenting information to facilitate high-quality decision-making
Session C: Pragmatic clinical trials (PCT) - challenges and innovations in getting informed consent
Session D: Delivery room research and the challenges for informed consent & Moderators panel
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 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.