Unifying Clinical, Quality
and Regulatory
TESARO drives end-to-end processes
with Veeva Development Cloud.
Veeva Development Cloud
Veeva Development Cloud brings together applications for clinical, regulatory, and quality to help organizations eliminate silos and drive end-to-end business processes across product development.
Today, product development applications are siloed and not well integrated. Multiple systems create inefficiencies and slow down critical business processes. Veeva is the first and only company to offer suites of unified applications on a single cloud platform across the entire product lifecycle.
With all applications on the Veeva Vault Platform, companies can streamline product development information across regions and departments for greater efficiency and compliance.
BENEFITS
- Faster time-to-market: Increase operational efficiencies by driving consistent, end-to-end product development business processes on a single system.
- Global alignment: Gain visibility across headquarters, sites, and countries.
- Comprehensive compliance: Achieve reliable information quality across the development lifecycle.
Data Management
Operations
Transforming how the industry captures and uses clinical data.
A fast, modern, and adaptive solution purpose-built for trial processes to speed critical workflows and enable real-time access to clean data.
Run the trial you want.
The only suite of unified clinical operations applications on a single cloud platform.
The industry’s first and only suite of unified clinical operations applications—including CTMS, eTMF, and study start-up on a single cloud platform—to accelerate trial execution, and deliver real-time visibility.
Enable proactive trial management.
Enable active eTMF for real-time inspection readiness.
Accelerate time to site activation.
Modernize quality management while driving compliance and operational innovation.
Seamlessly manage your quality processes and content with the Vault Quality suite of applications. All parties have access to a single authoritative source, enabling greater visibility and control.
Easily manage all quality processes.
Ensure compliance and role-based qualification.
Document control for all GxP documents.
Vault RIMBring speed and agility to your regulatory team with unified RIM.
Manage the planning, execution, and oversight of all regulatory activities within a single, unified RIM platform.
Manage product registrations globally.
Speed submission development.
Automate publishing during submission development.
Archive published dossiers securely in the cloud.
