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Medrio is a cloud based electronic data capture platform for clinical trial and registry studies.  It includes several features that go beyond most EDC software, handling complex study designs, and yet is user built without programming.  It is a secure platform currently used by pharmaceutical companies for FDA industry trials and is 21 CFR Part 11 compliant. 

Medrio includes a sophisticated query management system, as well as integrated missing form and missing visit reports to facilitate data quality.  It handles one-to-many (relational) structures to easily capture lists, diary, and grid data.  It includes tools for coding MedDRA classifications and open ended text, and includes integrated lab reference ranges.  It exports native datasets (SAS, SPSS, Stata) and has a controlled 3 stage (Dev-Test-Live) deployment.   Finally, it includes mobile technologies for in-clinic as well as remote patient reported outcomes and consent.

UC Licensing

Medrio is a software as a service (SaaS) could based platform.  Medrio has an active agreement in place and discount pricing that apply at all UC Campuses. 

Contact:

UCSF contact: Mike Schembri, [email protected] (415-353-7161)

Medrio contact: Jay Lomakin, [email protected] (415-276-9232)