eConsent Solutions

  1. Full Visibility For Study Teams And Control Over Consent 9/16/2025

    Enhancing patient comprehension and giving study teams full visibility and control over consent throughout your trial.

  2. eConsent For Clinical Trials 6/4/2025

    Electronic informed consent for patient-centric decentralized clinical trials.

  3. 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.

  4. 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.

  5. Just The Facts: Direct Data Capture 5/20/2022

    Start enabling direct data capture (DDC), clinical outcome assessments (eCOA), patient reported outcomes (ePRO), and eConsent with the Clinical ink platform.

  6. One Home for Sites™ Partnership Program Guide 4/7/2024

    Learn how your organization can become part of One Home for Sites, the only platform that’s bringing the industry together to help sites survive and thrive, along with their patients.

  7. 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.

  8. A Clinical Research Toolset That Delivers Power And Ease Of Use 1/23/2024

    Improve experiences and outcomes in clinical trials with a robust, and modern toolset of best-in-class solutions for eSource, ePRO, data capture, reporting, and more.

  9. EDC: Control Your Data, Control Your Study 2/16/2023

    Streamline data, maximize efficiencies, tighten up costs, and reach end goals faster using Medrio’s powerful and intuitive EDC tool.

  10. 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.