Patient Data Reporting Products/Services

  1. EHR-To-EDC Integration 2/27/2023

    Discover why more life science teams are using OpenClinica Unite™ to automate source data acquisition from patient medical record systems to clinical trial research databases and case report forms.

  2. 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.

  3. 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.

  4. How Can You Simplify Disclosure Compliance For Global Clinical Trials? 1/17/2025

    The most widely trusted solution for clinical trial disclosure management

    Managing clinical trial disclosures can be tedious and error-prone, opening the door to noncompliance. TrialScope Disclose provides a better way.

    Our centralized platform automates data entry and reporting for Clinicaltrials.gov, CTIS, and more. This reduces manual effort so you can focus on bringing new treatments to patients, not paperwork.

  5. Greenphire Clinical Finance Suite: Budgeting Benchmarking 9/16/2025

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

  6. eTMF: Promising Accessibility, Compliance, And More 5/28/2024

    Our model combines the depth and experience level of our people with effective tools and processes already in place that are designed to ensure your critical eTMF documents and content are secure, organized, readily accessible, and always in complete compliance with all relevant regulations.

  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.