Veeva CDMS is built for today’s clinical trials, eliminating technology limitations so you can design and run the trial you want. Innovative design tools speed the build process and eliminate manual steps. A next generation interface for data review helps CRAs work quickly and accurately and eliminates time spent paging through forms. Veeva CDB, a clinical data platform for aggregation and cleaning, provides a complete and concurrent view across all your study data.
Where to Start: System Overview for Veeva CDMS
CDMS Validation Packages: Veeva CDMS Validation Packages
The following tables outline Veeva’s processes specific to the CDMS product and CDMS services:
CDMS Product Processes
| Record Type | Document |
|---|---|
| Work Instruction | CDMS BRD Development WI (QV‑08118) CDMS Product Lifecycle WI (QV‑08117) |
CDMS Services Processes
For more information on Veeva’s Services, please see Veeva Services