Patient Data Reporting Solutions

  1. Adding eCOA To RTSM: Simplifying Workflow For Sites 12/9/2024

    Simplify trials with Signant’s integrated SmartSignals eCOA and RTSM. Eliminate duplication, reduce reconciliation, and streamline operations for faster, error-free studies.

  2. A Modern Clinical Research Platform 4/17/2025

    Explore a platform supporting secure integration of real-world data (RWD) from EHRs and tokenization, enabling rich, longitudinal insights, and flexible study designs.

  3. Elevate Your EDC With Integrated eCOA Capabilities 1/16/2024

    Utilize this eCOA module within the Signant SmartSignals Unified Platform to take advantage of a flexible and modern application designed for convenient at-home completion.

  4. Precise, Consistent, Faster Medical Coding For Clinical Trials 1/5/2026

    Rave Coder provides medical coding for verbatim terms from Rave EDC and external sources using the MedDRA, WHODrug and JDrug dictionaries. Rave Coder centralizes and streamlines medical coding, delivering key benefits to sites, coding specialists and data managers.

  5. Rave EDC: Trusted For Decades. Leading Today. Innovating For Tomorrow 1/13/2025

    Explore an EDC platform designed to simplify clinical trials, offering single sign-on, real-time data validation, and drag-and-drop eCRF creation.

  6. Why Choose TrialKit For Your Clinical Trials? 7/18/2024

    TrialKit supports everything from small biologics trials to large Phase 3 pharmaceutical trials and extensive registry studies, allowing you to capture and manage your clinical trial data as you see fit.

  7. Site Enablement Platform For Top Biopharma 8/1/2023

    Activate real-time clinical trial management with the only software with 95% site adoption. Create a digital connection to every site in your study on a platform they already love and use in their workflows.

  8. Optimizing The Path To RSV Vaccine Approval 2/20/2024

    Vaccine trials pose unique challenges; that's why sponsors and CROs trust us to navigate complexities and capture audit-ready, high-quality evidence required to get new vaccines to patients.

  9. Selecting And Evaluating An eRegulatory Solution 10/6/2023

    Take advantage of this checklist for evaluating eRegulatory solutions for clinical trial offices.

  10. IQVIA's Integrated IRT eCOA Platform 4/25/2023

    Improve study quality, accelerate decision making, and reduce site and sponsor burden by using IQVIA’s integrated Interactive Response Technology and electronic Clinical Outcome Assessment solution.