IQVIA Digital Site Suite

  1. Crowdsource UAT: An Opportunity For Future Validation 6/28/2023

    IQVIA, a leading health information technology and clinical research company, has introduced a new validation model for eTMF patterned after approaches used within the larger tech space.

  2. Reduce Workloads And Improve Insights With Crowdsource UAT 6/28/2023

    Learn to expedite UAT through objective evidence exchange, decreased individual workloads for participating sponsors, increased access to users, and faster, more reliable testing.

  3. Achieving Faster, Simpler Validation Through Crowdsource UAT 6/28/2023

    An approach most often seen in the larger tech space, crowdsource UAT can offer several potential advantages for the clinical trial industry and eTMF validation.

  4. eTMF As A Factory: Elements For High-Volume, High-Quality Processing 4/17/2023

    In an ideal scenario, the eTMF would operate like a well-oiled factory. Examine some of the key factors that would support making “The eTMF Factory” a reality.

  5. Use Our Experts For eTMF Management, Monitoring, And Maintenance 3/14/2023

    IQVIA eTMF Expert Services provide on-demand resources to help manage, monitor, and maintain eTMFs. Dive into the ways these services can improve productivity and ensure compliance.

  6. Securely Archive And Lock Down Your eTMF While Providing Inspector Access And Ensuring Ongoing Compliance 3/14/2023

    Trying to archive a TMF delivered by a CRO? Need out of non-compliant file systems? Interested in reducing archival costs? Discover how IQVIA eArchive could be the solution for these issues and more.

  7. Industry-Leading Tech And First-To-Market Innovations Optimizes eTMF 3/14/2023

    While an eTMF can be custom-configured upfront to meet the specific demands of a study, learn how IQVIA’s eTMF delivers the most advanced and sophisticated features and functionality available today.

  8. 3 Key Functions Your eTMF Needs To Meet New EMA Regulations 6/23/2022

    The European Union Clinical Trial Regulation No. 536/2014 recently introduced the most significant changes to the processes for clinical trial applications in at least the past 15 years. Learn how this impacts the Trial Master File and consider three key functions that an electronic TMF must have to achieve compliance and maintain organizational success.