On-Demand Data Management Webinars

  1. AI Meets Informed Consent: Opportunity, Risk, and What IRBs Need to See 5/14/2026

    Expert perspectives on IRB oversight, health literacy, and research ethics offer practical guidance to strengthen consent, protect participants, and align compliance with real-world research.

  2. CSA Gap Assessment 5/12/2026

    Learn how life sciences organizations are shifting from CSV to CSA using risk-based validation, automated testing, supplier leverage, and AI-ready compliance strategies.

  3. Applying AI to Study Simulation: From Design to Analysis 5/12/2026

    See how AI-generated synthetic patient populations can mirror real trial outcomes, enabling teams to test assumptions, refine protocols, and anticipate variability early — helping reduce risk, cost, and time while improving study design decisions.

  4. Accelerating Clinical And Drug Development Timelines With AI 5/8/2026

    This presentation brings together perspectives from across the industry to explore how AI is being applied today to improve clinical project management and unlock new opportunities in drug discovery.

     

  5. Medical Monitoring Oversight And Real-Time Data In Clinical Trials 5/8/2026

    Explore how real-time access to safety data is changing medical monitoring, with insights into continuous analysis, remote data visibility, and what these shifts mean for protecting patients.

  6. The Site-First Playbook: Best Practices For Successful EHR To EDC Adoption 4/21/2026

    This webcast highlights the benefits of streamlined data integration, reduced manual entry, and improved operational efficiency in clinical trials and the importance of collaboration.

  7. Unlocking The Promise of Digital Health Technologies In Clinical Trials 3/23/2026

    Discover the scientific, regulatory, and operational hurdles slowing digital health in clinical trials — and how design, guidance, and validation improvements are moving adoption ahead.

     

  8. Practical ICH E6(R3) Oversight For Your Centralized Monitoring Strategy 3/17/2026

    Bridge the gap between fragmented data and ICH E6(R3) compliance. Learn to use unified data signals to catch consent errors and enrollment delays before they trigger audit findings.

  9. Emerging AI Capabilities That Are Reshaping Scientific Workflows 3/9/2026

    Explore how AI‑powered search, intelligent data capture, and ontology‑driven structure streamline scientific discovery and documentation, as well as how structured data unlocks smarter analysis.

  10. Measuring Treatment Tolerability In Oncology: Expert Panel Discussion 2/19/2026

    Learn how to synthesize individual symptomatic data into a comprehensive narrative of tolerability, ultimately enhancing the clinical value and regulatory positioning of your oncology assets.