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. BYOD Is Here To Stay 5/3/2022

    In this webinar, eCOA experts will explore how to implement a BYOD strategy, relevant BYOD regulatory considerations, and where the market is going from here.

  3. Step Inside IQVIA One Home for Sites™ 1/28/2025

    Whether you're a sponsor, site, or technology vendor, now is the time to embrace One Home and join this industry-wide collaboration.

  4. Building One Home for Sites 7/23/2024

    Watch this presentation and demonstration of One Home for Sites for the latest updates on how the industry is coming together — even competitors — to alleviate the technology burden on research sites.

  5. Exploring Modular Mobile And Web ePRO 10/17/2023

    Review the capabilities of this collection of ePRO applications, available on both web and mobile platforms, for enhancing hybrid or decentralized clinical trial experiences.

  6. Proven Practices For ePRO Adoption 12/8/2022

    Industry experts discuss how a medical device company implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.

  7. Benefits Of Leveraging Real World Data (RWD) To Conduct Long-Term Follow Up 8/24/2022

    In this webinar, panelists discuss how connecting sources of real world data (RWD) to clinical trial enables many benefits, including the ability to supplement data for patients lost to follow up and augment trial data to help explain non-responders and adverse events.

  8. Are You Ready For Fully Remote eCOA In Your Next DCT Trial? 12/16/2022

    Watch to learn how you can build a better data management and compliance monitoring plan for your COAs in your next DCT trial.

  9. The eTMF As A Regulatory Standard 6/1/2023

    Discover essential insights on maintaining a high-quality Trial Master File (TMF) in a discussion about ICH GCP Essential Documents and the different regulations that apply to the TMF.

  10. Navigating The Journey Towards "Future-Proof" Clinical Data Assets 5/3/2021

    During this educational webinar hosted by Xtalks, data experts from ActiGraph and Koneksa Health present a roadmap to help clinical trial sponsors and their partners design and implement a “future-proof” raw data strategy to maximize the long-term value of digital biomarker data.