Webinar series · Nov–Dec 2026Emerging CDISC Standards: From Study Design to Analysis Results
Want to learn the new CDISC standards: USDM, AC, and ARS/ARD?
Join our standards leaders for a free 3-part live webinar series with practical guidance on adopting each standard. See how structured study definitions and analysis results transform modern clinical trial delivery.
What we'll cover
Session 1 · November 12, 2026
11:00 AM EST / 5:00 PM CET
USDM in Practice: Building Computable Study Definitions
How the Unified Study Definitions Model turns the protocol into machine-readable metadata, the foundation for downstream automation.
What this session covers
- The purpose and structure of USDM
- How protocol metadata drives downstream specifications and processes
- How USDM connects to Biomedical Concepts and AI-enabled study planning
Session 2 · December 3, 2026
11:00 AM EST / 5:00 PM CET
Analysis Concepts & Derivation Concepts: Transforming the Statistical Analysis Plan
How AC and DC capture analysis intent as reusable, machine-readable metadata.
What this session covers
- How a structured SAP differs from a narrative SAP, and why you keep both
- What is analyzed (AC) and how it is derived (DC), as reusable metadata
- How analysis intent flows directly into programming and reporting
Session 3 · December 12, 2026
11:00 AM EST / 5:00 PM CET
ARS & ARD: The Future of Analysis Results and Clinical Reporting
How the Analysis Results Standard and Analysis Results Data make outputs traceable, reusable and metadata-driven.
What this session covers
- ARS architecture and metadata-driven TFL generation
- Why results held as data replace static RTF and PDF files
- Connecting ARD to review, AI and CSR authoring, plus implementation best practices
Why this series
Clinical workflows still move through hand-offs: protocol, SAP, specifications, programming, TFLs and the CSR. At each step the same intent is re-read and re-created by hand. Emerging CDISC standards make that intent machine-readable, so it can flow downstream with traceability built in and give AI something structured to work from.
This series is about practice, not theory: what each standard does, where it fits, and how to adopt it without disrupting the work you are already doing.
Meet the speakers
Bhavin BusaPrincipal & Co-Founder, Clymb Clinical · CDISC ARS Product Owner & Co-Lead
Malan BosmanLead Automation Engineer, Clymb Clinical
Richard MarshallPrincipal Data Standards & Automation Architect, Clymb Clinical · CDISC ARS Principal Data Modeler
Save your seat
Register once for the full series, or pick the sessions that fit your role.