PATIENT DATA REPORTING WHITE PAPERS & ARTICLES

PATIENT DATA REPORTING APPLICATIONS & STUDIES

PATIENT DATA REPORTING PRODUCTS & SERVICES

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

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.

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

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.

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.

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.

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.

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.