Clinical Technologies Solutions

  1. Endpoint Quality Solutions For Schizophrenia Trials 8/29/2023

    Gain a deeper understanding of these innovative solutions by downloading the brochure below, designed to provide insights into how Signant's specialized offerings can significantly enhance the landscape of schizophrenia clinical research.

  2. Cut Your Study Build Times By Up To 50% With eCOA 8/24/2023

    Improve study start-up experiences with flexible deployment options, a groundbreaking global instrument library, and dedicated services and support offered by Medidata’s eCOA.

  3. IQVIA Feasibility 9/27/2022

    Employing a digital, data-first strategy, IQVIA Feasibility brings together survey data, confidential disclosure agreements (CDAs) and site intelligence data, enabling sponsors to efficiently collect vital information while improving the site experience.

  4. Your Partner For Simplified Site Operations And Maximized Returns 11/13/2025

    With dedicated CTA Negotiation, Site Payment, and Financial Analysis experts, we reduce site burden and optimize study execution so your team can focus on delivering exceptional research as care.

  5. eCOA And ePRO Solutions For Clinical Trials 3/10/2025

    Planning to launch a patient-centric decentralized clinical trial? Give your clinical trial patients an app that makes it easy to participate—from anywhere at any time.

    Simplify clinical trial participation with an integrated eCOA and ePRO solution

    TrialKit’s electronic clinical outcome assessment (eCOA) and electronic patient-reported outcomes (ePRO) platform integrates with all currently available wearables, mobile operating systems, and web applications. Whether you collect data in the clinic, with provisioned devices, or take a bring-your-own-device (BYOD) approach, you can count on seamless data sharing and efficient study execution.

  6. Driving Efficiency And ROI In Clinical Trials 11/19/2024

    Integrate sensors into your study to evaluate digital endpoints with a comprehensive solution that accelerates drug development, reduces patient sample sizes, cuts costs, and improves patient insights.

  7. Streamline Trial Master File Documentation And Integrate With Sites 6/12/2025

    Streamline your Trial Master File (TMF) documentation and integrate with study sites to accelerate trial timelines.

    Other eTMFs promise ease of use and seamless integration with the sites eISF, but they can’t deliver 100% adoption.

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

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

  9. Revolutionize The Way You Conduct Clinical Research

    Clinical Conductor CTMS maximizes trial revenue with robust finance management, participant-centric clinical trial management, oversight tools, and more.

  10. 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.