E-Technologies STREAM

  1. Vault Safety-EDC Connection 6/24/2024

    Learn how to automate the flow of Serious Adverse Event (SAE) information between data management and safety systems, enabling more timely responses by Pharmacovigilance (PV) teams.

  2. Document Processing: A New Hope 8/8/2024

    Tired of slow, error-prone document processing? Discover how top companies are boosting speed and accuracy while slashing costly rework. Watch now to learn how you can achieve TMF excellence faster.

  3. Optimal eCOA For Vaccine Trials 8/23/2023

    Delve into the pivotal role that technologies like electronic Patient-Reported Outcomes (ePRO) can play in generating substantiating evidence and streamlining vaccine trial operations.

  4. 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.

  5. 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.

  6. 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.

  7. End-To-End Clinical Data Flow 6/24/2024

    Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.

  8. 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.

  9. 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.

  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.