ePRO/eCOA Services & Products

1. 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.

2. 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.

3. 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.

4. 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.

5. TrialKit eCOA/ePRO 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.

6. Make Participating In Your Clinical Trial Easier Than Ever 2/20/2025

   The success of clinical trials depends on patient participation.

   But patients and caregivers need reliable support first.

   Being part of a trial is often nuanced and time-consuming. Archaic travel, antiquated payment processes and card fees are not only frustrating, but can also chip away at the reimbursement funds participants are owed.

   This isn’t what you want for your participants, but you haven’t had a better choice. If we have the technology to make things better, we should. So we are.

   Mural Link is the clinical research industry’s first participant management platform, designed to meet the needs of modern-day participants, help them enroll and remain in a trial, and reduce the administrative burden for sites.

7. Ergomed's Risk-Based Quality Management 2/6/2025

   Ergomed’s Meticulous Risk-Based Quality Management Approach

   As a pioneer in providing comprehensive support for your clinical research, Ergomed champions an innovative Risk-Based Quality Management (RBQM) approach. This forward-thinking strategy ensures the highest patient safety standards, regulatory compliance, and data reliability. Ergomed’s proactive approach to managing clinical trials tackles clinical research complexity head-on.

8. Streamline Electronic Data Capture With iMednet EDC 1/22/2025

   At the core of our comprehensive eClinical platform, iMednet EDC is uniquely designed to help sponsors and CROs achieve their clinical research goals. Highly flexible, it enables you to build studies quickly, while easily adapting to complex protocols and mid-study changes with ease.

9. How iMednet Addresses Key Industry Challenges 1/22/2025

   In today’s complex clinical research landscape, sponsors and CROs face numerous challenges that can impact study timelines, costs, and data quality. The iMednet platform offers innovative solutions to address these critical issues.

10. 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.