Case Study: Clinical Trials Research Group (CTRG) achieves accelerated study timelines and submission-ready data with Medrio

How CTRG Streamlines Complex, Multi-Site Clinical Trials

Clinical Trials Research Group (CTRG), a CRO with more than 120 cumulative years of ophthalmology experience, faced a complex, multi-site trial comparing two distinct treatment groups with varied and adjustable schedules. To manage this dynamic design and ensure submission-ready data, CTRG partnered with Medrio and used Medrio CDMS/EDC and RTSM along with Medrio’s data management and biostatistics services.

Medrio provided a consultative study build, RTSM treatment-group configuration, eCRF templates, UAT, real-time data cleaning, CTMS integration, and risk-based monitoring, which streamlined workflows and reduced administrative burden. As a result, CTRG shortened study build times from about 16 weeks to 10–12 weeks, improved site efficiency, and decreased database lock time—delivering operational excellence, accelerated timelines, and consistently high-quality data.

Clinical Trials Research Group

Crystal Gates

Director of Clinical Operations