The benefits to your patients and your team are plentiful. Removing the patient burden of always coming into the clinic increases recruitment, compliance, and patient engagement. Plus, the ability to stay in close contact with patients regardless of location diversifies participant populations and allows very ill patients to participate. The accessibility of secure mobile devices increases patient expectations making electronic collection no longer just preferred, it is expected.
Our easy-to-use technology is streamlined to improve data quality and study oversight offering simplicity without compromise. With over 15 years of experience, our decentralized platform is a proven and trusted solution designed to meet the needs of your clinical study design – whether it be traditional, hybrid, or virtual.
We designed our technology to be flexible and with the end-user in mind. No custom integrations are required, allowing you real-time access to clinical and patient-reported data, which results in faster insights and improved patient safety. Whereas paper sources require weeks to transcribe and input into the EDC, data captured electronically via our ePRO, eConsent, and Direct Data Capture solutions funnel into the EDC in real-time, eliminating transcription error cleaning and speeding up patient data trend analysis.
We also understand that it’s not just about using the right technology – you need a team of experts you can trust and depend on to build your study quickly and monitor progress along the way. Our professional services team provides everything you need to be set up for success. Our onboarding programs, eLearning training, project management, and custom reporting offerings leverage our in-house experts to ensure that you are fully supported at all hours every day.
We know the patients are what drive the industry – in many respects they are harder and harder to reach. There is a tremendous potential to truly realize patient accessibility with a decentralized clinical trial model.