E-Technologies STREAM

  1. Auto Generate Documentation 4/2/2025

    Unlock seamless software development with IQVIA’s eCOA, which automates screenshots, validation documentation, and audit trails, ensuring real-time updates, easy exports, and full traceability.

  2. Accelerate EDC Data Entry For Your Sites 2/22/2024

    Discover how you and your sites can benefit from Rave Companion, an easy-to-set-up and user-friendly tool that fits right into existing data entry workflows, ensuring simpler, quicker, and more accurate data entry.

  3. 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.

  4. 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>

  5. An AI Action Plan For The TMF Professional 6/12/2024

    Explore AI's impact on TMF processes in this on-demand webinar. Gain clarity on AI's potential, key evaluation criteria, and practical applications for enhancing TMF health and inspection-readiness.

  6. Industry-First eTMF AI: PhlexTMF v21 4/6/2023

    Pre-trained on millions of documents and embedding the cumulative guidance of Phlexglobal’s TMF experts, uncover how teams can ensure clinical documents are “right-first-time” at document upload.

  7. Maximize Control And Transparency On The Path To Study Go-Live 10/10/2024

    Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.

  8. Reduce TMF Misfiles & Metadata Errors With Next-Gen AI-Enabled eTMF 4/17/2023

    Listen in as Chief Product Officer Jim Nichols, Product Manager Jim Horstmann, and VP Solutions Consulting Aaron Grant discuss issues and solutions for trial master files.

  9. Deploy eConsent Around The World With Confidence 8/16/2022

    Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.

  10. Study Build And Scheduler Tools 3/27/2025

    Empower your study participants with IQVIA eCOA’s tailored user experiences, flexible event triggers for clinicians, comprehensive training resources, and 24/7 support for seamless study management.