On-Demand Webinars

  1. ePRO's Impact On Patient And Site Journeys 5/15/2024

    Join our solutions experts as they demonstrate how Castor ePRO can enhance your clinical trial by improving the patient experience and streamlining site operations.

  2. Three Data Trends to Consider Now When Developing Your Decentralized Clinical Trial Strategy 5/23/2022

    In this free webinar, learn how to update your clinical data strategy that ensures you can scale trials globally while decreasing the overall burden on sites and patients.

  3. 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.

  4. Facilitate Widespread Outpatient Immunotherapy Treatments With DHTs 6/6/2025

    An expert panel explores how the industry leverages digital innovation to manage immunotherapy risks and critical next steps toward deploying scalable, technology-driven CRS monitoring solutions.

  5. Future Of Digital Biomarker Platforms In Parkinson's Research 4/21/2023

    Understand the importance of platform-enabled real-time data capture and how to leverage AI and machine learning platforms to drive study insight into disease progression and treatment.

  6. Accelerating Clinical Trials Through Streamlined Confidential Disclosure Agreements 2/9/2026

    In this presentation, Dr. Christine Senn addresses the persistent challenge of study startup delays by focusing on a primary legal hurdle: the Confidential Disclosure Agreement (CDA).

  7. 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.

  8. The Revival Of Electronic Informed Consent 11/2/2022

    The clinical research industry has been reluctant to adopt eConsent for several reasons. Unearth how the industry should continue exploring and implementing digital technologies in earnest in the future.

  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. 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.