On-Demand Webinars

  1. 3 Ways To Unlock The Value Of Real-World Evidence 12/13/2022

    Tune in as Castor’s Director of Solutions Consulting Kristen Harnack illustrates how a modular approach to clinical technology can help you conduct an RWE study.

  2. Addressing Opportunities And Challenges In Digital Health Data 10/22/2024

    Experts from diverse industry sectors unpack key points from the FDA’s final guidance on Digital Health Technologies (DHT) for remote data collection in clinical investigations.

  3. A Dive Deep Into Castor's eConsent 11/16/2023

    Discover how digital consent is working to enhance diversity, empower participants with education, drive quality data, and streamline operations.

  4. The Art Of Accelerated Study Closeout: End Of Study Solutions 11/2/2023

    Watch as experts from eClinical Solutions and Medidata delve into end-of-study process challenges, the transition to electronic distribution and management, the advantages of leveraging a digital platform, and more.

  5. 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.

  6. Agile eConsent: Taking A Flexible Approach To Global Implementation 6/28/2022

    Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.

  7. 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.

  8. The New Vaccine Race: Why A Decentralized Approach Wins 3/29/2022

    What does it take to get vaccine trials up and running quickly and efficiently? As it turns out, the best answer is DCT. Learn why in the available webinar.

  9. 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.

  10. How FAIR Data Principles Power Clinical Analytics Success 11/8/2023

    Explore key challenges in accessing and preparing analytics-ready clinical data, how FAIR guiding principles can help maximize the value of clinical trial data, and the impact of innovative analytics.