For more information about CDISC webinars, please fill out our contact form here.
PLEASE NOTE: All listed webinars are in US Eastern time, unless otherwise indicated.
TMF Reference Model General Meeting - Q3 2025 (Japan/Asia Pacific)
Join the TMF Reference Model Q3 General Meeting! We’re hosting live sessions to connect our global community. Choose the session that fits your time zone:
Agenda & Speakers
- General Announcements | Paul (Fenton) Carter
- Events & US Interchange Update | Karen Roy & Jamie Marie Toth
- Community Update | Jamie Marie Toth (US/Europe), Yuto Kanda (China/Japan)
- TMF V4 Updates | Donna Dorozinsky
- Working Group Updates:
- ICH E6 R3
- Vendors & Metadata
- Medical Device
- Computerized Systems
- EU CTR
- ISF Initiative: Jamie Marie Toth
- Education | Dawn Niccum
- Risk Initiative
- Real-World Evidence
Don’t miss this opportunity to stay connected, informed, and engaged with the TMF global community.
Language
English
Join the CDISC Open Source Alliance (COSA) and open-source developers as they showcase free tools on 23 September!
Presentations & Presenters:
• USDM to SDTM TS Domains – Berber Snoeijer, CDISC
• Smart Submission Dataset Viewer – Jozef Aerts, XML4Pharma
The "Smart Submission Dataset Viewer" allows to inspect CDISC SDTM, SEND and ADaM submission files in the modern CDISC Dataset-JSON 1.1 standard format.
• Dataset-JSON Viewer – Sebastià Barceló Bauçà & Hugo Signol, Cytel
• VDE Dataset Viewer – Dmitry Kolosov
• Upcoming Hackathons – Bhavin Busa, Clymb Clinical & Charles Shadle, CDISC
Don’t miss this chance to:
• Explore cutting-edge open-source tools
• Hear directly from the developers
• Get inspired to contribute to community-driven innovation
Language
English
The future of medical device trials is being built on interoperable, high-quality data. In an effort to streamline processes and accelerate innovation, the Medical Device Innovation Consortium (MDIC), in partnership with the Clinical Data Interchange Standards Consortium (CDISC) and the FDA, is leading an initiative to develop data standards for in vitro diagnostic (IVD) devices.
This session, led by clinical data experts, will highlight the significant progress being made. The panel will share key insights from the recently published landscape analysis and discuss:
- Historical challenges and current state for the definition and adoption of standards
- Ongoing efforts between CDISC, FDA, MDIC, and the industry toward the creation of IVD clinical data standards
- What should be done to align global regulatory expectations to simplify the submission and review process
Join us to learn how these standardization efforts are creating an end-to-end harmonized platform that will shape the future of clinical trials for IVDs.
Speakers:
- Carey Smoak, Co-founder and Co-leader of the CDISC Device Team, Roche (retired)
- John Owen, Head, Project Management Office, CDISC
- Nick Decker, Head of Regulatory Policy, Roche
Moderator:
John Acampado, MBA, MPH, PMI-ACP, Sr. Director Clinical Strategy, Veeva Systems
Presented by: MDIC, Veeva, and CDISC
Organized by: Medical Device Innovation Consortium
Language
English
Join open-source developers from the CDISC community as they showcase their free tools as part of the CDISC Open Source Alliance (COSA). Learn how you can leverage these tools to facilitate the implementation of CDISC standards in your systems. Stay tuned for more specific details about what the team will cover in this spotlight!
Agenda TBA
Language
English
Join us for our Quarterly TMF Webinar!
Stay informed with the latest updates from the TMF Steering Committee and community. Don’t miss this opportunity to engage, ask questions, and stay up to date on key TMF developments.
Language
English
TMF Reference Model General Meeting - Q4 2025 (Japan/Asia Pacific)
Join us for our Quarterly TMF Webinar!
Stay informed with the latest updates from the TMF Steering Committee and community. Don’t miss this opportunity to engage, ask questions, and stay up to date on key TMF developments.
Language
English