Pharmaceutical companies
Veeva Vault is an industry-leading, unified cloud platform designed exclusively for pharmaceutical, biotech, medical device, and life sciences organizations. It enables teams to manage regulated content, streamline quality processes, centralize regulatory operations, and ensure global compliance across the product lifecycle.
Built specifically for the life sciences ecosystem, Veeva Vault delivers end-to-end visibility, faster workflows, and audit-ready documentation, making it one of the most trusted enterprise platforms for highly regulated industries.
Veeva Vault ensures full visibility, streamlined workflows, and audit-ready compliance for life sciences organizations.The platform is designed to meet global regulatory standards:
Every action is tracked through automated audit trails, ensuring full transparency for inspections.
Veeva Vault integrates AI-powered automation to help teams:
Veeva Vault connects seamlessly with
This ensures that the right teams always access updated, approved, compliant content.
Teams across regulatory, quality, medical, clinical, and commercial functions can collaborate in real time.
Veeva Vault brings all documents, digital assets, quality records, regulatory files, and medical content together in one secure environment.
A compliant promotional content management system for MLR reviews, digital assets, and multi-channel promotional materials.
Designed for medical affairs teams to manage scientific content, FAQs, response documents, and medical communication workflows.
Controlled document management system (DMS) for SOPs, training documents, and quality procedures with full compliance.
Manages quality processes including deviations, CAPAs, complaints, audits, and change control.
End-to-end regulatory information management for submissions, labeling, registration tracking, and regulatory operations.
Supports clinical trials with eTMF, study documents, site files, and clinical trial workflows.
Unified pharmacovigilance platform for safety case management, signal detection, and regulatory safety reporting.
Eliminates content duplication and outdated files by maintaining a centralized, compliant repository for all regulated content.
Automated workflows streamline content movement from creation to approval, significantly reducing review timelines.
Every action is fully recorded, version-controlled, and traceable, ensuring continuous compliance and inspection readiness.
Gain real-time visibility across regions, teams, and product portfolios for better decision-making and governance.
Supports R&D, clinical, regulatory, quality, medical, and commercial teams on a single unified platform.
Veeva Vault is ideal for
Pharmaceutical companies
Biotechnology organizations
Medical device manufacturers
Contract research organizations (CROs)
Contract manufacturing organizations (CMOs/CDMOs)
Life sciences service providers
We help you implement, customize, and optimize Veeva Vault to align with your workflows. Our expertise includes
System configuration
Workflow automation
Content migration
Integration with CRM and ERP systems
Training and user enablement
Compliance validation support
Veeva Vault gave us complete control over our regulated content. All documents are easy to find, properly versioned, and always inspection ready. It has brought a lot of clarity to our daily work.
Our review and approval cycles became much faster after moving to Veeva Vault. Automated workflows reduced back and forth and helped teams focus more on quality instead of manual follow ups.
Content migration and system setup were handled very professionally. The solution was configured around our processes, which made user adoption much easier.
Different teams like quality, regulatory, and medical now collaborate smoothly in one system. Veeva Vault removed silos and improved transparency across departments.
Working with Cloud Rank on Veeva Vault was a great experience. They took time to understand our compliance needs and configured the system so we are always inspection ready.
Founder
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Located in India
