Patient Data Reporting Solutions

  1. Rave Lite For Phase I Trials 9/12/2024

    Discover a flexible, cost-effective platform tailored to Phase I studies, providing rapid, efficient study builds, seamless transitions, and scalable solutions for early-stage clinical research.

  2. Streamlined Deployment And Patient Data Collection 7/31/2025

    Navigate the inherent complexities, infinite variables, and constant changes that define life-sustaining studies with confidence using a patient-centric platform.

  3. IQVIA eArchive 5/21/2021

    Whether you’re archiving a TMF delivered by your CRO partner, looking to move out of noncompliant file systems, or interested in reducing the high costs of archiving in your active eTMF, IQVIA eArchive is the rapid deployment solution for you.

  4. Technology And Scientific Expertise To Power Your Program 8/5/2024

    Learn how our expertise in eCOA, RTSM, and eConsent solutions can accelerate your drug development program from early phases to regulatory approval.

  5. Assess And Optimize Ratings Reliability 8/30/2023

    See how this centralized solution for clinical ratings enhances the precision and dependability of data obtained from assessments based on clinician-reported outcomes (ClinROs), thus achieving elevated data quality.

  6. IRT And eClinical Technology Considerations For Cell And Gene Therapy 8/20/2021

    Don't try to fit cell and gene therapy studies – or any kind of study – into pre-defined functionality. The Cenduit IRT and Quantum Interactive™ agile design platforms and reporting tools support clients’ most complex requirements.

  7. Rave RTSM: Bringing Innovation And Convenience To IRT 2/3/2026

    Built with the end user in mind, our solution enables teams to reach key milestones more efficiently, adapt quickly to evolving trial needs, and keep studies on track from start to finish.

  8. EDC For Medical Device Clinical Trials, Diagnostics Studies 1/6/2026

    Through centralized clinical data and seamless application integration, this EDC platform provides powerful cross-study and cross-functional insights that support faster, more informed decision-making.

  9. Hybrid eConsent: Remote And On-Site 3/21/2025

    Studies show when participants are informed and comfortable with the consent process, they're more likely to comply with protocol, remain enrolled, and contribute to faster study deployment.

  10. ePRO For Oncology Studies 5/15/2024

    Now introducing a customized ePRO solution designed specifically for oncology studies: a user-friendly app with a streamlined two-step onboarding process.