On-Demand Webinars

  1. The Strategic And Scientific Imperative For Prospectively Generated Real-World Evidence 11/7/2022

    This webinar will explore the RWE/RWD landscape and focus on those situations in which a prospective observational study or registry presents a more optimal solution.

  2. Key Considerations For A Direct-to-Patient Clinical Trial 1/20/2022

    This webinar explores important considerations for developing a Direct-to-Patient strategy and the RTSM features needed to support its execution.

  3. Navigating The RWD Landscape In Japan 1/12/2023

    Take a deep dive into the current system and database utilized in Japan and delve into tips for database selection and how it should be selected according to target disease area and desired result.

  4. Building An Analytics Culture In Clinical Development 3/28/2024

    Discover how embracing fast and flexible clinical analytics can help you address clinical questions and provide real-time insights into data issues as they arise.

  5. 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.

  6. Address Unmet Measurement Needs In Parkinson's Disease With Wearable DHTs 8/15/2024

    Review the latest advancements in wearable digital health technologies (DHTs) and how they are poised to address these challenges and advance treatment options for patients with movement disorders.

  7. No Code Requirement: Pre-Trial Insights For Operational Success 5/14/2024

    Discover how a no-code solution transforms insight generation from weeks to minutes. Learn to run analyses, test hypotheses, and enhance patient trial recruitment and diversity with ease.

  8. Examining The "Why" And "How" Of Integrating Your eTMF And CTMS 6/24/2022

    As requirements for improved inspection readiness and quality risk management become more critical, discover the need to create a seamless integration and data flow between the eTMF and CTMS.

  9. Accelerating Clinical Data Review With Traceable Workflows 4/17/2025

    Discover how streamlined workflows and enhanced collaboration between data managers and medical reviewers can boost clinical trial efficiency, improve data quality, and ensure patient safety.

  10. Qualified eSignature in Electronic Consent Systems 2/25/2026

    This on‑demand session offers a clear, practical overview of the major eSignature types used in eConsent — ranging from simple electronic signatures to fully qualified electronic signatures — and explains when each is appropriate.