Veeva Clinical Data Help
Veeva EDC
With Veeva EDC, your organization can design and administer a study, from initial data collection and review to study closeout. Veeva EDC also includes modules for subject randomization and the management of lab data and normal ranges.
Veeva Coder
With Veeva Coder, clinical coders can quickly code medical terms using the WHODrug or MedDRA dictionaries. Vault can also autocode terms that are exact matches to dictionary entries or known synonyms to reduce manual coding requirements.
Veeva CDB
Veeva CDB assembles all your study data into a consistently formatted data lake, where data managers can clean it, report on it, and export it. This complete and current data helps you make faster, make better decisions, and run more effective trials.
Veeva eCOA
Veeva eCOA (electronic Clinical Outcome Assessments) is a cutting-edge solution to simplify the design, management, and completion of eCOA for sponsors, sites, and patients. It captures questionnaire responses directly from clinical trial patients (ePRO), clinicians (eClinRO), or patient caregivers (eObsRO) through an app or webpage.
