Veeva Vault 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 Vault CDMS

CDMS Validation Packages: Veeva Vault 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

Record Type Document
Procedure CDMS Project Implementation SOP (PS-00551)
Work Instruction CDB Implementation and Configuration WI (PS-00723)
CDMS Customer Acceptance WI (PS-00234)
CDMS Periodic Review WI (PS-00228)
CDMS Production Access WI (PS-00508)
CDMS Project Design WI (PS-00571)
CDMS Project Implementation WI (PS-00551)
CDMS Project Initiation WI (PS-00233)
CDMS Project Verification WI (PS-00235)
CDMS Site and User Management WI (PS-00155)
CDMS Study Closeout WI (PS-00227)
CDMS Study Conduct WI (PS-00241)
CDMS Study Data Extract WI (PS-00168)
CDMS Study Deployment WI (PS-00425)
CDMS Training and Curriculum Development WI (PS-00231)
CDMS Utilities Administration WI (PS-00299)