Ease
of Translation
Users can translate clinical data between different
data management systems.
Ease of Conversion
Researchers can convert “homegrown”
or proprietary systems data to the industry standard
Operational Data Model
(ODM) format.
Ease of Submission
Sponsors can submit data to the FDA in CDISC SDTM/SDS
format.
Enhanced Prospective
Analysis
Sponsors can perform prospective analysis and
cross-pooling of clinical trial data.
Ease of Exchange
CROs can exchange clinical data with
the trial sponsor based on industry standard formats,
such as CDISC’s Operational Data Model (ODM)
and Logical Data Model (LDM) markup standards. |
- Adhere to industry-standard data formats
- Reduce the tediousness of data integration
- Save time by streamlining your data
exchange
- Reduce the burden of data management
- Add more flexibility to your information
system
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