The Virtual 2021 CDISC Europe Interchange will be held over two and a half days, 28 - 30 April. This year, the Europe Interchange and CDISC TechniCon will be combined into a single event, and attendees that register for the Europe Interchange will gain access to the TechniCon - get two conferences for the price of one!
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.
The webinar will provide compelling reasons why clinical investigators as well as technical colleagues stand to benefit from using standards, even for just one study, even if it’s observational.