Medrio for Early Phase Pharma
and Biotech Trials
Organizations conducting early phase pharma and biotech clinical research need an easy and flexible eClinical solution to accelerate their trials. See how Medrio, the market leader in EDC and eSource for the early phases, can be that solution for you.
Succeed in Your Early Phase Clinical Research
Medrio’s eClinical platform was built to deliver the speed that fast-moving, time-sensitive early phase pharma trials demand. Pharma and biotech companies everywhere use Medrio’s EDC, DDC, ePRO, and eConsent solutions to leverage robust eClinical functionality at a low cost of ownership. These researchers have eliminated unnecessary complexity in their Phase 1 clinical trials and beyond, and accelerated the market arrival of life-saving medical products. No wonder, then, that Medrio is outgrowing the early phase market by a large margin.
Medrio’s intuitive software empowers you to build your studies and make mid-study changes yourself – without relying on external parties. With full control of your processes and a 24/7 Support team in your corner, there’s no limit to what you can achieve in your next study.
Build studies in an average of 2.8 weeks with no programming required. Make mid-study changes with no downtime, copy forms and visits for re-use, and streamline your clinical data monitoring. These efficiencies empower you to get your databases locked sooner and accelerate the delivery of new treatments.
Our project-based pricing lets you select modules a-la carte, so you only pay for what you use. And with Medrio’s robust training and support resources, you can keep timelines down and reduce study costs as a result.
eClinical Platforms for Success in the Early Phases
Keep study build and mid-study changes fast, easy, and in your control. Leverage cutting-edge modules like dictionary coding and randomization. Ensure data quality with real-time edit checks. And do it all on an innovative, fully-compliant EDC platform.
With Medrio’s innovative DDC platform, you can capture source data directly into a tablet app that comes pre-integrated with our EDC. This gives you the power to drastically reduce the burden of source data verification and streamline your monitoring.
Accelerate your consenting process and improve your compliance with our innovative tablet application. Medrio eConsent makes comprehension easier for subjects and streamlines operations at sites.
With Medrio’s web-based ePRO application, you can stay better attuned to the patient experience, as well as cater to patient convenience by allowing patients to fill out PRO surveys via email from the comfort of their own homes.