EDC/Data Management White Papers & Case Studies

  1. Unified Platform Supports Rapid Implementation Of Rescue Study 1/17/2024

    Explore how these integrated solutions helped an emerging biopharma to implement a plan for study build and migration with minimal disruption to sites.

  2. eSource For A COVID Treatment Trial 1/17/2024

    Unearth how this emerging biopharmaceutical company was able to overcome challenges to successfully facilitate a Phase 2 trial for a COVID-19 treatment in critically ill patients.

  3. Emerging Biopharm Rapidly Sets Up Phase 1 Oncology Trial 1/16/2024

    Uncover how an emerging biopharmaceutical company was able to expedite the initiation of a Phase 1 oncology trial for a novel treatment targeting relapsed/refractory multiple myeloma.

  4. Unified, Integrated eClinical Research Solutions 1/16/2024

    Facilitate efficient digitalization and optimization of clinical trials that meet the unique needs of small and mid-size biopharma organizations with the Signant SmartSignals Unified Platform.

  5. An EDC/DDC Solution For Modern Clinical Trials 1/16/2024

    Utilized in over 3,000 clinical trials, learn about this comprehensive EDC solution that delivers high-quality data on time and addresses any study team's goals.

  6. Technology Solutions And Services Tailored For Emerging Biopharma 1/16/2024

    Explore how this collection of solutions and services is transforming clinical trials and empowering emerging biopharma organizations to revolutionize medicine.

  7. How Can Phase 1 Trials Employ eClinical Solutions? 1/8/2024

    Uncover how this unified platform is helping sponsors and CROs generate high-quality data, accelerate trials, and rapidly scale to Phase 2 and beyond.

  8. eClinical Platform Accelerates COVID-19 Treatment Trial By 2 Weeks 1/8/2024

    Examine a COVID-19 treatment trial that utilized integrated EDC, eConsent, eCOA, RTSM, and TeleVisit solutions, all within a single platform, to address three critical challenges.

  9. How MAC Clinical Research Innovates With CDMS/EDC 12/27/2023

    Discover how a partnership with one of Europe’s largest contract research organizations exemplifies the crucial role that technology plays in the realm of clinical studies.

  10. Rave TSDV - Improve CRA Efficiency And Reduce Site Burden 12/20/2023

    Source data verification (SDV) is a critical activity within clinical trial monitoring, yet the traditional approach focused on 100% SDV is limited in its ability to quickly identify issues and prevent them from recurring. Rave TSDV (Targeted SDV), unified with Rave EDC, enables CRAs to focus on critical to quality (CtQ) factors identified within risk management activities.