Compliance Without Compromise: How to Ensure EHR Data Integrity
At the AMIA Informatics Summit in 2025, researchers shared their promising EHR-to-EDC findings. They assessed five oncology trials across diverse...
Reimagining the Protocol for the Future of Research
The protocol is the brain of a study. It’s time we gave it a digital body.” In clinical trials, the...
EHR to EDC: A Short Demo
Chris Weiss, OpenClinica’s Vice President of Sales, recently led a short, live demo of our Unite EHR-to-EDC eSource solution. In...
How to Know You’re Ready for EHR to EDC Integration
To refresh your memory, EHR-to-EDC integration, also known as EHR eSource, is the process of combining electronic health records (EHR)...
EHR-to-EDC: Choosing the Right Solution for Clinical Trials
Integrating electronic health records (EHR) with electronic data capture (EDC) systems can dramatically enhance data accuracy, workflow efficiency, and decision-making...
You Asked and We Answered: What is EHR-to-EDC in Clinical Trials?
Let’s start with a definition: EHR to EDC, also known as eSource and EHR-to-EDC integration, is the process of combining...
EHR to EDC Integration: Get the Data 15 Times Faster
I recently had the opportunity to talk with Allison Proffitt, Editorial Director of Clinical Research News, about EHR to EDC...
Eight Ways Medical Device Clinical Trials Differ from Drug Trials
About two million medical devices in 7,000+ categories are on the market. According to the Food and Drug Administration (FDA),...
Registry Studies Are Unique: 8 Distinct Features
The primary purpose of registry studies has traditionally been to collect data to better understand long-term trends in specific populations....
Award Winning Solution Solves Big Pain Point for Clinical Trials
ICYMI, OpenClinica’s award-winning platform eliminates the expense and errors associated with manual abstraction of electronic health record (EHR) data into...