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. 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.

  3. Better Experiences And Faster Startups 8/22/2022

    By combining electronic form workflows and interactive question-and-answer sections, this eConsent solution optimizes ICF processes to offer improved patient and user experiences.

  4. End-To-End Digital Therapeutics Studies Powered By Technology 2/2/2023

    Curebase offers a variety of decentralized study models designed and tested for any type of DTx trial.

  5. 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.

  6. 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.

  7. Electronic Informed Consent For Clinical Research 2/16/2024

    We partnered with leading academic medical centers, sponsors, hospital systems, and site networks to create an eConsent platform that is easy-to-use and minimizes risk.

  8. Unlock Additional Capabilities For Your Next Clinical Trial 2/21/2023

    Gain insight on how a single point of entry can improve patient and site experience by offering best-in-class eCOA, consent management, and patient engagement solutions.

  9. The Path To Proof, Reimagined 5/15/2024

    By combining technology with clinical and operational expertise, Signant Health prioritizes the clinical research stakeholder experience, making it more intuitive, while ensuring the data journey is direct.

  10. 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.