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SEND Virtual Meetings: Public Broadcast Hosted by FDA

CDISC invites you to an FDA-hosted public broadcast during the SEND Team’s fall virtual meetings. The broadcast is an opportunity for stakeholders to stay informed on what’s going on with the development of SEND and its use in regulatory submissions, as well as hear from our global SEND user community.

18 October 2023 10:00 – 11:30 am EDT

Data Standards and ePRO Systems: A Road Less Travelled?
The CDISC Open Rules Engine (CORE): Open-Source Software For Clinical
Clinical Data Interchange Standards Consortium (CDISC) and the Multi-Regional Clinical Trials Center of Brigham and Women’s Hospital (MRCT Center) collaborate to offer plain language clinical research definitions as a new standard.
Austin, TX and Boston, MA – 24 Mar 2023 – Clinical research is essential for the discovery of new treatments and medical interventions that advance public health and medicine. Yet clinical research is complex, and scientific concepts are often complicated to explain.
TMF Reference Model Affiliation With CDISC Could Improve TMF Interoperability
CDISC and conect4children (c4c) release of Paediatrics User Guide to facilitate better medicines for babies, children and young people

Austin, TX and Newcastle upon Tyne, UK – 22 Feb 2023 – CDISC and conect4children (c4c) have announced the release of a Paediatrics User Guide, freely available on the CDISC website, to facilitate the development of medicines for children.

CDISC Welcomes New Chair and Members to Board of Directors
Austin, TX – 10 January 2023 – CDISC today announced three members have joined its Board of Directors: Jonathan Chainey, Dominic Labriola and Rhona O’Donnell each began serving a three-year term at the beginning of the year. Existing Member, Dr. Erik Pulkstenis, now leads the Board as Chair.
Veeva’s Dan Crawford Elected Chair of CDISC Advisory Council
AUSTIN, TX and PLEASANTON, CA — Dec. 14, 2022 — Veeva Systems (NYSE: VEEV) and CDISC are pleased to announce that Dan Crawford, Veeva Clinical Database (CDB) principal consultant, has been elected chair of the CDISC Advisory Council (CAC) . The CAC comprises representatives from CDISC platinum members who play an important role in shaping CDISC’s development and direction, providing the CDISC executive team with recommendations that support CDISC goals.
Clupea, KIT to establish Korea's 1st CDISC standard-based non-clinical big data…
SEND Virtual Meetings: Public Broadcast Hosted by FDA

CDISC invites you to an FDA-hosted public broadcast during the SEND Team’s fall virtual meetings. The broadcast is an opportunity for stakeholders to stay informed on what’s going on with the development of SEND and its use in regulatory submissions, as well as hear use cases from our global SEND user community.