VEEVA DEVELOPMENT CLOUD
Technology Foundation for
Product Development
Eliminate data and process silos across
clinical, quality, regulatory, and safety.
Veeva Development Cloud
Veeva Development Cloud is the technology foundation for product development that brings together applications for clinical, quality, regulatory, and safety to help organizations drive end-to-end business processes.
Today, product development and manufacturing systems are not well integrated, which creates inefficiencies and slows down critical operations. Veeva is the first and only company to offer unified suites of applications that are connected on a single cloud platform. This enables organizations to centralize content and data across global departments for greater efficiency and compliance. To learn more, hear from biopharmas on Veeva Development Cloud or visit Veeva Vault Platform.
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.
Vault Clinical Operations
Vault Clinical Operations streamlines processes, eliminates data silos, and enables real-time visibility. Make smarter decisions, reduce costs, and bring therapies to market faster.
Enable real-time inspection readiness.
Proactively manage trials.
Pay clinical research sites faster.
Accelerate time to site activation.
Randomize patients and manage trial supplies.
Automate information sharing.
Streamline and automate training.
Centralize clinical trial disclosures.
Veeva Clinical Data
Speed and simplify study timelines with modern applications for clinical data. Veeva Clinical Data connects the data flow across patients, sites, and sponsors.
Veeva's clinical data systems help teams collect, clean, and manage trial data with agility and speed.
Collect, validate, and verify study data.
Aggregate, clean, and transform clinical data from multiple sources.
Capture data directly from trial patients, clinicians, or patient caregivers.
Improve patient experience.
Vault Quality
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.
Simplify postmarket surveillance for medical devices.
Document control for all GxP documents.
Manage and execute paperless validation.
Deliver the right content to the shop floor.
Ensure compliance and role-based qualification.
Accredited GxP eLearning courses.
Optimize QC labs for batch release.
Vault RIM
Bring 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.
Automate publishing during submission development.
Speed submission development.
Archive published dossiers securely in the cloud.
Vault Safety
Veeva Vault Safety is the only modern application for the intake, management, and real-time oversight of adverse events.
Real-time management and oversight for adverse events.
Centrally manage pharmacovigilance content.
Vault Connections
Vault Connections are Veeva-delivered integrations that seamlessly transfer data and documents between clinical, quality, regulatory, safety, and commercial Vaults. They are designed to streamline cross-functional business processes by breaking down silos, providing greater visibility, and automating manual tasks. For more information on Vault Connections, visit our Resource Hub.
Share product, study, and site data and documents.
Speed change control and variation management.
Get up-to-the-minute site enrollment information.
Shorten submission timelines.
Top Companies Use Veeva
Resources for Veeva Development Cloud
How can Veeva Help Your Business?
