CDISC standards in practice: Challenges, gaps, and the cost of getting it wrong

Across the industry, teams still face challenges in implementing standards consistently, aligning systems, and avoiding costly downstream issues. From late-stage rework to submission delays, the gap between theory and execution can have significant consequences.

Watch the the webinar “CDISC standards in practice: Challenges, gaps, and the cost of getting it wrong” where we explore how CDISC standards work in real-world clinical trial environments, beyond theory and guidelines.

In practice, the biggest challenges rarely come from the standards themselves, but from how and when they are implemented. Misalignment between systems, fragmented data flows, and late standardization decisions often create hidden inefficiencies that only surface at the most critical stages of a study. These issues are often underestimated until they result in delays, increased workload, or regulatory complications.

Through expert discussion, we will unpack where processes break down, why these issues occur, and how organizations can better align data, systems, and teams from the start. The session will also highlight how early decisions around data structure and standardization directly impact study efficiency, regulatory readiness, and overall trial success. This webinar is designed for clinical data professionals, data managers, biostatisticians, and decision-makers looking to improve both data quality and operational efficiency.

What you’ll learn

• How CDISC standards are applied across real clinical trial workflows
• Where the most common challenges and gaps occur
• The true cost of late-stage data issues and rework
• Lessons learned from real project experience
• What needs to change to improve efficiency and outcomes

Meet the speakers

• Urosh Viliimanovich, Chief Customer Officer, Wemedoo
• Caslav Vojvodic, Head of Integration, Wemedoo

Moderated by:

Valérie Czaya, Chief Operating Officer, Wemedoo