On-Demand Webinars

  1. The Cutting Edge Of Pharma: AI And RWD 1/19/2024

    Taken from a spotlight session at the CNS Summit, gain insights from thought leaders from Norstella and Citeline regarding artificial intelligence and real-world data.

  2. Secrets To A Collaborative Model To Improve TMF Management 10/30/2023

    Speakers from Phlexglobal and Regeneron share the benefits of their highly effective partnering model and lessons learned that you can apply in your organization.

  3. 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.

  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. Leveraging DHTs To Improve Data Collection And Analysis 2/25/2025

    How can wearable DHTs be leveraged to measure physical activity in patients with immunological diseases, enhancing clinical trials and advancing drug development?

  6. 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.

  7. Accelerate Parkinson's Drug Development With Active, Passive DHT Monitoring 4/15/2025

    Discover how a new ActiGraph–Indivi partnership is enhancing neurology clinical trials with digital health technologies that enable more sensitive, real-world outcome measures.

  8. 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.

  9. 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.

  10. Designing ePRO and eConsent Solutions that Participants and Sites Want 10/26/2022

    Participant-focused eClinical technologies offer significant potential to decrease paper-based processes and improve end-user experiences in collecting patient-reported outcomes (PRO) and informed consent, but many users continue to experience rigid technology, complicated hardware provisioning processes, and clunky implementations that leave sponsors, CROs and sites questioning the value.