Discover how Yonalink simplifies data capture, management, and transfer. Reduce the burden on your team while improving, data quality, oversight, and control over your trials.
Faster data, better results.
Stream clinical trial data securely, in real time, from various sources, including patient questionnaires, electronic diaries, medical devices, wearables, and EHRs.
Let Yonalink’s unrivaled AI-driven data mapping solution populate your patient data from the site’s EHR to the proper fields in the Yonalink EDC without cumbersome and time-consuming manual data mapping.
Get high quality data when it’s collected, not weeks later.
Quality and quantity. You can have both.
The volume, variety, and velocity of clinical trial data are increasing exponentially, increasing data quality concerns and transfer time. By automating today’s manual data transfer process, Yonalink enables study sponsors to accommodate today’s data volume and to seamlessly incorporate additional data points as needed, without increasing site burden, transfer times or compromising on data integrity.
You asked, we answered.
We pioneered EHR-to-EDC streaming to significantly reduce the need for manual data transfer. But we didn’t stop there: to meet the research community’s need for a more holistic, scalable approach to clinical trial data management, Yonalink offers a single end-to-end platform that includes an AI-powered EDC, eConsent, eCOA, ePRO, and more. Eliminate the need for multiple systems and reduce training times, costs, and operational complexity. Yonalink improves trial efficiency so that your team can focus on what matters most – advancing your clinical trials.
We make you look good.
Sponsors rely on CROs like yours for expert guidance in sourcing innovative, cost-effective resources to expedite clinical trials. We’ve got you covered with a comprehensive, intuitive solution for clinical data collection and management that seamlessly integrates into sponsor and site workflows for all types and phases of studies, across all therapeutic areas, in every part of the world.
EHR-to-EDC data streaming
Simple and flexible protocol setup and amendments
Powerful edit checks, display rules, and auto-calculated fields
Better data oversight
Greater data quality
Improved trial efficiency
A one-stop-shop for your one-stop-shop.
You provide all the clinical trial services for your clients. We provide all the data collection and management solutions for you. With Yonalink, your sponsors will benefit from incomparable EHR-to-EDC data streaming. They’ll also get eConsent, ePRO, eCOA, and a top-of-the-line EDC in one easy-to-use platform.
Say goodbye to data silos and hello to the convenience of data collection, management, and transfer in one intuitive platform.
Increase productivity, increase staff satisfaction.
Between juggling patients, data capture, input, and analysis, study coordinators have a lot going on. Yonalink eases these burdens by automating data transfer between medical centers and trial sponsors.
A robust, flexible, and easy-to-use EDC
Easy protocol configuration and amendments
Automatic CRF field calculations
Side-by-side visit views
Bulk signatures of CRFs by PIs
With less time devoted to data copying and analysis, your staff can allocate their resources more effectively to focus on higher-priority tasks.
Easy to set up, even easier to use.
Yonalink streams data from thousands of medical centers across the globe. Contact us to see if your hospital is already integrated into the Yonalink network.
If necessary, integrating Yonalink into your hospital’s IT stack is quick and painless; there’s no need for new hardware or expensive software. Integration can be completed in as little as two weeks, confirming our commitment to provide a solution that is user-friendly for study coordinators and your hospital’s IT team as well.
Think that’s fast? With Yonalink, new studies can be set up within a day or two, instead of the weeks often required by most other EDCs.
Real-time data streaming
EDC, ePRO, eCOA, eConsent, and more, in one convenient platform
Seamless protocol amendments
IP allocation and randomization
Attract more sponsors and top researchers by providing them with the tools and connectivity they need to collect, transmit, and analyze clinical data easier than ever.