How CTRG Streamlines Complex, Multi-Site Clinical Trials

Managing complex, multi-site trials is no easy task. Clinical Trials Research Group (CTRG), a CRO with 120+ cumulative years of ophthalmology-specific experience, needed flexible study management solutions to support their sponsor’s multi-site trial comparing two distinct treatment groups.

To uphold data quality standards and maintain operational excellence, CTRG chose Medrio.

In this downloadable case study, see how CTRG utilizes Medrio CDMS/EDC, RTSM, and Clinical Data Services to achieve:

38% faster build times
50% eCRF utilization
90% real-time data cleaning

Contributing experts at Clinical Trial Research Group (CTRG) include:
Crystal Gates, Director of Clinical Operations
Jess Norton, Lead Clinical Research Associate (CRA)

Complete this form to download this Case Study.

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