ePRO/eCOA White Papers & Case Studies

  1. Signant SmartSignals® RTSM Overview 9/18/2024

    Discover how Signant SmartSignals® RTSM streamlines complex trial management with modern features, efficient design, and advanced reporting capabilities—far beyond traditional systems.

  2. Medable Studio 9/16/2024

    More than just a builder, Medable Studio offers unmatched control over study creation and launch, eliminating the common roadblocks of study startup and empowering users throughout the process.

  3. 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.

  4. Overcoming Participant Compliance Challenges In A Medical Device Study 9/9/2024

    Uncover how Catalyst Clinical Research enhanced participant compliance and streamlined scheduling for a TENS device study using the TrialKit platform, with crucial support from CDS.

  5. A Fast, Customizable, And Cost-Effective ePRO/eCOA Solution For Complex Studies 8/29/2024

    Complex studies often require costly customizations and lengthy timelines. Learn how our innovative study designer can streamline study launch, save you time, and reduce costs.

  6. Fulfilling MDR Requirements For A Groundbreaking Microsurgery Robot 8/19/2024

    Discover the help a company pioneering the field of open surgery received to advance their robotic technology, replacing their former EDC system to improve their clinical research efficiency.

  7. DTx Company Leverages Real-World Evidence Platform In Registry Study 8/19/2024

    Discover how Castor’s eClinical system enabled a groundbreaking study in behavioral disorder treatment to collect Real-World Evidence (RWE) to support product research and claims.

  8. SmartSignals Streamlines eClinical Workflows 8/16/2024

    With robust APIs, detailed guides, and real-time monitoring, Signant SmartSignals Marketplace enhances eClinical workflows, minimizing duplication and ensuring reliable data across systems.

  9. 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.

  10. Capture And Transfer Up To 100% Of EHR-Based Data 7/23/2024

    Flatiron Clinical Pipe™ eliminates manual data entry of structured and unstructured data—improving site workflows, lowering data monitoring costs, and enabling you to hit study milestones faster.