E-Technologies STREAM

  1. Right-Size Your eConsent Approach 11/17/2023

    Delve into the art of tailoring the eConsent experience to match your study and patients' specific needs, such as crafting eConsent documents, selecting appropriate delivery models, and more.

  2. Closing The "Compliance Gap" In TMF Archiving 8/15/2022

    Discover how organizations are crossing this “compliance gap” with PhlexTMF for Viewing, an easily accessible TMF archive for internal use, audits, and inspections.

  3. Addressing Site And Sponsor Challenges In Digital Trials 10/10/2023

    <p>While the digital transformation of clinical trials has made tremendous strides in recent years, the plethora of new technologies can overwhelm. Learn how to help sites and sponsors combat the overload of technology.</p>

  4. Introducing eCOA+ Streamlined Evidence Generation 1/16/2024

    Watch as Colin Weller, Vice President and General Manager of the Digital Outcomes and Evidence Platform at Medable, Inc., articulates the vision for eCOA+ and the trajectory of evidence generation.

  5. IQVIA eCOA: Amplifying The Patient's Voice 4/19/2024

    Dive deep into the capabilities of IQVIA's eCOA with our expert Edward Bartels. He will focus on how to effortlessly create a diary, schedule site/participant assessments, and intuitively manage translations and compliance.

  6. Technology Overload: Addressing Site Challenges Of Digital Trials 5/23/2024

    Watch as speakers explore the experiences of sites conducting digital and hybrid trials, discussing the critical benefits of a change management strategy and a unified digital trial platform.

  7. 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.

  8. IQVIA eCOA Scribe Application 3/27/2025

    Experience seamless, secure, and flexible eCOA data collection with our application designed for diverse users, compatible with multiple devices, and equipped with offline functionality and robust authentication.

  9. Introducing A Smarter, More Cost-Effective Way To Run Clinical Trials 3/13/2025

    While early-phase trials often rely on less capable, cost-effective systems, the transition to more complex studies in later phases necessitates a more robust EDC system.

  10. Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations 2/22/2023

    Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.