Seamlessly connect data for sites, patients, sponsors
Veeva Clinical Data brings together the core data collection and processing capabilities needed for the added complexity of device and diagnostic trials. It simplifies and standardizes data collection, reconciliation, and processing for all stakeholders.
-
Reduce effort for sites and sponsors
Veeva EDC unifies data entry, image management, auto-coding, and study design optimization. Veeva also offers sites free software, such as VeevaID, to give clinical researchers a single sign-on experience.
-
Simplify participation for patients
Veeva eCOA streamlines data collection from clinical trial patients, clinicians, or patient caregivers in a single platform that works on any device or web. Patients can complete consents and access trial documents throughout study conduct.
-
Automate data reconciliation and review for sponsors
Veeva CDB provides a single place to aggregate and clean all clinical study data. Data managers have complete and concurrent data at their fingertips for efficient database lock activities.
Products
Veeva Clinical Data
Veeva Clinical Data applications are integrated to allow for one flow of data, ending up in a clinical database for aggregation and cleaning. A unified suite, it enables seamless interactions between sponsors, sites, and patients.
Veeva EDC
Electronic data capture application for sponsors to collect patient data from sites and ensure quality.
Veeva CDB
Central environment to manage all data for a trial, including aggregating, cleaning, and transforming clinical data from multiple sources.
Veeva eCOA
Captures responses from patients, caregivers, and clinicians using an app or webpage, and provides sponsors an easy way to build surveys and distribute to sites.
40%
faster study startup
50%
faster study builds
60%
faster study closeout
