ePRO/eCOA Services & Products

  1. Suvoda eConsent 9/16/2025

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

  2. Suvoda eCOA 9/16/2025

    Delivering high-quality patient outcomes data with patented technology, rapid deployment, and expert guidance.

  3. Budgeting And Benchmarking 9/16/2025

    Generate accurate study budgets faster with the industry’s most contemporary fair market value (FMV) data for investigator grant costs.

  4. Castor-eCOA Clinical Trial Technology 8/21/2025

    1,735 eCOA & ePRO Studies Completed 

    eCOA and ePRO with Enrollment, eConsent, Payments and EDC integrated. Our services cover build, licensing and 24/7 support.

    95%+ Patient Compliance Rate

    4-8 Weeks to Deploy

    190+ Validated Instruments

  5. Electronic Data Capture (EDC) System: Leverage Flexibility And Speed 8/11/2025

    Neither traditional nor hybrid clinical trials can operate on rigid EDC systems.

    They require flexible data collection systems that support protocol amendments without downtime and accept mobile data without hassle. As a cloud-native solution, TrialKit bends to accommodate mid-study changes. And as the first full-featured EDC platform available as a native mobile app, TrialKit flexes to meet the demands of traditional, hybrid/decentralized, and completely remote clinical trials.

    Give your team the freedom to build, deploy, and manage their studies, their way—weeks faster than with rigid EDCs and for a fraction of the cost of the major players.

  6. eCOA: Delivering High-Quality Patient Data 7/31/2025

    Purpose-built with users at the center to make it easier and more efficient to get quality patient outcomes data for submissions and approvals.

    Collecting quality data on patient outcomes is often one of the most important parts of a clinical trial. It is also challenging, and many eCOA solutions make it feel even more difficult with complicated processes, lack of questionnaire reusability, slow set up, and difficult to use tech.

  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. Distribute, Monitor, And Exchange Study Documents With Every Site 6/12/2025

    Effortlessly distribute, monitor, and exchange study documents with every site—wherever they work, whenever they need it.

    Other tools promise site connections, but they can't deliver 100% coverage with a solution sites actually want.

    Adoption

    They claim sites use their tool…but you need sites to love it.

    Tracking

    They let you send documents…but you need to know the status of every document at every site.

    Integration

    They offer integration within their ecosystem…but you need compatibility with every site and sponsor software.

  9. eConsent For Clinical Trials 6/4/2025

    Help your patients make informed decisions without burying them in paper

    With electronic informed consent (eConsent) software, your patients can access consent forms using any device they choose. And because it’s part of TrialKit’s unified platform, both your patients and your study team get a seamless experience.

  10. Commercial Alerts: Now Available With EHR, Claims And Prescription Data 3/27/2025

    Identify & engage healthcare professionals (HCP) treating eligible patients—in near real-time

    Timely physician engagement is critical to therapy adoption. Quest Diagnostics combines near real-time lab data with other data sources including EHR, claims and prescription data to help pharmaceutical teams identify and connect with physicians managing eligible patients at key decision time point in the patient journey.

    In today’s competitive pharmaceutical landscape, ensuring that physicians receive timely, relevant information about new therapies is essential. Quest’s unique combination of industry-leading deidentified lab data, enhanced with claims, prescription (Rx), and EHR insights, allows pharma teams to refine targeting, optimize engagement, and drive better patient outcomes.