Legacy Data Conversion to CDISC Standards
We help convert legacy clinical trial data into CDISC-compliant SDTM formats, enabling regulatory submission support for older studies.
Before First Subject In
SDTMs finalized and submission-ready ahead of FSFV.
Within 4 Weeks
From Final Protocol Approval to live eCRF — faster study startup.
Within 12 Weeks
Last Subject Last Visit to Database Lock — rapid and reliable closure.
Our expertise covers:
Manual Mapping and Standardization
Custom mapping of non-standardized raw data to SDTM 3.3 when automation frameworks aren’t feasible.
Protocol Deviation Structuring
Specialized DV domain development to address inconsistently captured protocol deviations.
Time-Efficient Legacy Conversion
Agile turnaround on legacy dataset conversions—even under strict deadlines and complex data constraints.
Accelerate Your Trails With Us
With our innovative solutions, we empower healthcare providers to make smarter decisions and achieve long-term success.