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What is eSource in Clinical Trials? Let’s start with a definition of EHR eSource. According to the FDA, eSource is:…
ICYMI OpenClinica recently published a case study about our work with the Imperial College of London, Zero Interruptions: Migrating 14…
On November 30, 2022, ChatGPT was released for public use. A mere five days later, there were one million users.…
Mid-study data migrations are inherently complex, since any two electronic data capture (EDC) systems will have different ways of storing…
Clinical trial researchers and research coordinators are burned out. No wonder – we’re nearly four years into the COVID-19 pandemic,…
Change comes in oh so many forms in a clinical trial: Changes to form design, Changes to workflow, Changes in…
If you work in the clinical research industry, you have likely heard the term decentralized clinical trial, abbreviated DCT. While…
ICYMI, OpenClinica published a playbook, Fast-tracking clinical trials with eSource: Get to market faster and enhance site relationships. In the…
The purpose of informed consent is to ensure people are fully aware of what they would be signing up for…
A Q&A with CEO, Cal Collins Things are going great, and they're only getting better.…The future's so bright, I gotta…
To say I’m ecstatic about the impact of SMART on FHIR on the usefulness of real-world data in clinical research…
In the words of Heraclitus, the Greek philosopher, “Change is the only constant in life.” In my experience, the fear…
This spring members of the OpenClinica community are converging on London to learn, share, and collaborate with each other. I…
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