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As OpenClinica’s Co-Founder and COO, I had the pleasure of serving as the host for OC24, our annual global conference…
ICYMI, OpenClinica recently debuted market-leading automated study calendaring functionality. Our study calendaring capabilities automate scheduling and protocol visits and enable…
Oncology trials are among the most complex and challenging to conduct due to the variability in cancer types, the need…
It’s my privilege to share with you the article, Dissemination of CDASH eCRFs via the CDISC Electronic Case Report Form…
Looking to reduce data entry, errors and burnout among your clinical research coordinators? By all accounts, it’s not easy being…
On May 9, 2024, Taylor Swift took her Eras Tour to Paris. ICYMI, Swift commenced a two-year concert tour on…
I recently had the opportunity to talk with Allison Proffitt, Editorial Director of Clinical Research News, about EHR to EDC…
A surprising number of clinical trials take advantage of the opportunity to try our EDC system for clinical trials –…
Interest in participating in a clinical research study is increasing, according to a global survey of 12,000+ conducted by the…
At OpenClinica, we frequently write about the benefits of eSource EHR integration. That’s because it’s been, and continues to be,…
About two million medical devices in 7,000+ categories are on the market. According to the Food and Drug Administration (FDA),…
This June in Boston, we’ll be hosting OC24, our OpenClinica user group conference. We debuted our annual in-person event 15…
How EHR eSource drives efficiencies across sites & sponsors In the words of one clinical research coordinator, “Entire Monday mornings…
The primary purpose of registry studies has traditionally been to collect data to better understand long-term trends in specific populations.…
We all hate duplicate work. Why do we make our clinical research sites do so much of it? Electronic Case…
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