Date and Time:
THU 22 APR 2021, 11:00 AM - 12:30 PM Eastern US Standard Time
Join us we present the soon-to-be released CDASH SAE V2.0 Supplement. The purpose of this supplement is to 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.
This webinar will showcase the CDASH modeling for CDASH SAE Concepts. Additional information can be found here .
John Owen, Head of Partnerships and Development, CDISC
Webinar Language: English
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