Clinical Technologies Webinars

31. Clinical Leader Smart Sourcing Solutions Expo: Suvoda eCOA, Unified With IRT On The Suvoda Platform 9/9/2025

    Discover the unique advantages of Suvoda eCOA and IRT working together on a single, unified platform.

32. From Complexity To Clarity: Automate eCOA Configuration With AI 9/9/2025

    Clinical trials are more complex than ever, but building and launching global studies doesn’t have to be.

33. Clinical Leader Smart Sourcing Solutions Expo: Streamlining eCOA For Modern Clinical Trials 9/9/2025

    Explore an eClinical platform with a native mobile app for seamless data capture and study management, featuring advanced AI capabilities that deliver powerful analytics and reporting.

34. Clinical Leader Smart Sourcing Solutions Expo: Why Castor? 9/9/2025

    How do Agentic workflows (with human oversight) unlock data from patient-mediated medical records and convert clinical data and lab PDFs into traceable, submission-ready study data?

35. Clinical Leader Smart Sourcing Solutions Expo: Retention By Design 9/9/2025

    Enhance participant retention through intuitive UX and real-time site support tools, while seamlessly integrating with IRT, EDC, and third-party platforms.

36. Accelerate Clinical Insights: From Data Deluge To Decisions In Minutes 9/5/2025

    Unlock clinical trial insights in minutes, not months. Discover a platform that streamlines data review with AI-powered listings and visualizations to empower faster, smarter decisions.

37. Breaking Barriers With PCR: Innovative Solutions For Clinical Trial Success 9/3/2025

    This presentation brings together experts from Precision for Medicine, Avidity Biosciences, and Indaptus Therapeutics to examine the expanding role of PCR-based molecular monitoring.

38. Stop Protocol Amendments Before They Start 8/22/2025

    Julie Smiley of CDISC explains how digital protocols can revolutionize protocol feasibility by running eligibility criteria through EHR systems to identify potential patient populations up front. She discusses how this approach addresses the major cause of protocol amendments — patients not meeting eligibility criteria — and supports quality by design principles.

39. Breaking Free from 20 Years of 'Do Everything' Mentality 8/22/2025

    Joe Fitzgerald of Regeneron provides historical context for the regulatory evolution from ICH E6's original focus on thorough, consistent execution to the current emphasis on QbD. He explains how the industry is shifting from 100% SDV and exhaustive edit checks to early detection and prevention of high-impact errors, emphasizing the mindset change required for successful implementation.

40. How Digital Protocols Are Eliminating Manual Errors 8/22/2025

    Julie Smiley, VP of Data Sciences at CDISC, reviews CDISC's new 360i initiative, explaining how it transforms standards into structured executable metadata to automate clinical development processes. She discusses the USDM (Unified Study Definitions Model) and how digital protocols reduce ambiguity and minimize manual errors throughout the clinical trial lifecycle.