Castor Videos

  1. FDA's Vision On PRO Collection For RWE 9/24/2024

    In this presentation, a distinguished panel of experts illuminates the crucial role of patient-reported outcomes (PROs) in shaping regulatory decisions and drug development strategies, particularly in light of FDA expectations.

  2. The Impact Of An AI Enabled Consent Process 5/15/2024

    In this episode of Download with Derk, we take an in-depth look at our internal experiment where Castor Companion was utilized during the consent process.

  3. 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.

  4. From Paper To ePRO: Providing Flexibility And Efficiency 3/12/2024

    Explore the transformative impact of flexible ePRO technology on clinical trials, elucidating how it enhances patient-centricity and operational efficiency for sponsors.

  5. 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.

  6. 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.

  7. Navigating Successful eConsent Adoption From Sponsor To Site 10/17/2023

    Drawing inspiration from real-world instances within the pharmaceutical and medical device sectors, watch as industry experts unravel the pivotal role of eConsent in optimizing modern clinical trials.

  8. Patient-Centric Technologies And Tokenization In RWE Studies 5/17/2023

    Castor joins experts from United Biosource (UBC) and Datavant to discuss all things real-world evidence, patient-centric technologies, and the role of tokenization in clinical research.

  9. Efficiently Manage Clinical Data With Castor's EDC, CDMS 5/11/2023

    Effortlessly conduct multi-center clinical trials worldwide for drug development with Castor’s EDC and CDMS platforms, including eCOA, ePRO, EHR eSource, eConsent, and IRT modules.

  10. Deploying Studies Faster To Accelerate Clinical Research 12/13/2022

    Capture the world's clinical research data and integrate it seamlessly with other data in your clinical trial ecosystem, optimizing every trial activity in one centralized hub with Castor's EDC/CDMS.