SOLUTION SHEET Medrio for Medical Device Studies Flexible, cost-effective and right-sized clinical trial solutions The Medrio Difference for Device Trials Device Studies Medical Device Companies Customer Satisfaction Device trials demand speed and efficiency even as complexities increase. From regulatory challenges, to the growing number of new data endpoints—device researchers, sponsors, and CROs need nimble tools that streamline their IP development lifecycle. At Medrio, we’ve worked with over 180 leading device companies on 500+ studies, and we understand your need for agile solutions. Our integrated eClinical suite offers the flexibility and functionality to expedite the development pathway and bring your innovations to market faster than ever before

Reduce Your Study Timelines Build and deploy your device studies in a matter of days with flexible tools designed for fast data entry and data accuracy. With a few clicks of a mouse, device researchers can streamline query creation, deploy mid-study changes, and instantly upload bulk study data without technical support. And the best part? With access to reliable, high-quality data, your clinical teams can make proactive decisions that shorten your study timelines and streamline your product development. Our integrated eClinical suite of EDC, ePRO, eConsent, and DDC keeps your trials running...

How We Deliver Better Data for Medical Device Trials 7 ccess and share A real-time data from any device, anywhere and focus on UAT with pre-validated software and duplicate data with live edit checks and logic-based workflows snap with a host of on-demand queries, eCRFs, and custom reports to AE notifications, missing data alerts, and out-of-range result triggers Conduct Cost-Efficient Studies Costs keep steadily rising and now bringing a device to market can cost sponsors and CROs up to $500 million. Our transparent, subscription-based pricing model was designed to keep costs low in your medical...

Having a good EDC with online/offline data capture that can record data on a tablet is crucial. And there are not many vendors that can provide that.” Jenny Li, Senior Manager of Clinical Operations, inui Health Built-In Compliance Medical device trials rely on numerous information exchanges between sites, sponsors, study managers, and suppliers. Ensure your sensitive data is secure with pre-validated software, and keep pace with the changing regulatory landscape with an eClinical suite designed to improve patient compliance. Built-in compliance—Good Clinical Practice (GCP), 21 CFR Part 11 Compliance,...