Webinars address industry hot topics, best practices and challenges around implementing the standards, allowing attendees to learn from the CDISC community of experts. For more information about CDISC webinars, please reach out to us at cdiscwebinar@cdisc.org.

Date and Time:
TUE 10 NOV 2020, 11:00 AM - 12:30 PM Eastern US Standard Time


Join us as we discuss Public Review for CDASH SAE v2.0 Supplement.

CDISC, with support from our partner TransCelerate Biopharma, is developing version 2.0 of the CDASH SAE Supplement, which will capture how to structure serious adverse events (SAE) concepts for regulated clinical trials. It will also align with E2B (R3) Electronic Transmission of Individual Case Safety Reports (ICSRs) Implementation Guide – Data Elements and Message Specification and bring the standard up to date with current CDISC standards.

Public Review is a key quality step in the development of this supplement for the research community. We invite you to contribute your expertise.


John Owen, Head of Partnerships and Development, CDISC

Date and Time:

MON, 16 NOV 2020, 11:00 AM - 12:30 PM Eastern US Standard Time


Announcing the CDISC Certification program!

CDISC is currently rolling out the pilot version of the CDISC Certification exam. Join us to learn how and why we developed a certification program, why you should take the exam, and how you can sign up. We’ll also detail exam scope, what you can do prepare for it, and specifications of the pilot session.


Marine Laurent, COO, CDISC
Amy Palmer, Head of Standards Development, CDISC

Webinar Language: English

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