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) |