YPrime’s Platform Brings Vendor-Agnostic Integration to Clinical Trial Management
MALVERN, P.A. – June 14, 2017 – YPrime announced the release of YP Connect, a cloud-based platform-as-a-service (PaaS) integration solution for clinical trials. YP Connect incorporates a real-time open architecture to directly integrate data from eClinical systems.
Designed to replace time and labor-intensive processes involved with the organization and analysis of multiple data sources collected during a clinical trial, YP Connect centralizes and transforms data into common formats across eClinical capture systems. For clinical researchers, an intuitive user interface provides reporting and a cross-platform view of their clinical trial data. YP Connect’s core features include:
- Integration ability with a broad range of data sources across legacy and modern eClinical applications.
- Robust analytical capabilities provide the ability to identify trends and anomalies in operational performance and patient-level safety data.
- Role-based reporting provides customized data views from high-level summaries to individual data points.
- The integration platform-as-a service-model (PaaS) eliminates the need for sponsor-side integration infrastructure.
“YP Connect is the first of its kind in clinical research as a vendor-agnostic clinical data integration service. It connects incompatible eClinical systems, and brings critical information together in context,” said Shawn Blackburn, YPrime CEO and co-founder. “The multiple applications used for data collection have resulted in more fragmented sources of information, and less productivity. Information organization and visualization within dashboards gives researchers the ability to make informed decisions quickly and efficiently. Our clients rely on solutions like YP Connect to bring order to the chaos of clinical trial information management.”
About YPrime
YPrime offers more than a decade of focused work with eclinical systems to expedite and improve the quality of patient management, clinical supplies, drug accountability and clinical data. Cloud-based interactive response technology (IRT) and electronic clinical outcome assessment (eCOA) platforms enable greater speed, precision and integration in clinical trial management. Our data services tools help sponsors bring together fragmented clinical research data into contextual information they can act on. YPrime’s technology and service offerings enable sponsors to move faster and more efficiently to their next development milestone.
Contact:
Katherine Cloninger
Senior Director, Marketing
kcloninger@yprime.com
Empowering Sites and Patients: The Impact of Personalized Support in Clinical Trials
November 26th 2024To meet the growing demands of clinical research, sponsors must prioritize comprehensive support models, such as clinical site ambassadors and patient journey coordinators, who can address operational challenges and improve site relationships, patient satisfaction, and overall trial efficiency.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
FDA Finalizes Decentralized Clinical Trial Guidance
November 25th 2024The FDA's guidance is part of a broader effort to modernize clinical trials, improve efficiency, reduce participant burden, and expand access, particularly for underrepresented populations and those in geographically or economically constrained areas.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
