Veeva: Cloud Software for Life Sciences
Veeva helps life sciences, biotech, and MedTech companies manage R&D and commercial workflows. It is designed for organizations that need to maintain GxP compliance and digital document control.
At a glance
- Category
- Healthcare
- Best for
- Pharmaceutical companies, Biotechnology organizations, MedTech companies, Clinical research sites, Life sciences R&D teams
- Pricing
- SiteVault is free for research sites with up to 20 active studies. Pricing for larger sites is tiered. Buyers should confirm current pricing on the vendor website.
- Key use cases
- Clinical Trial Management, Regulatory Submission Planning, Quality Process Centralization, Pharmacovigilance, Digital Investigator Site Files
- Integrations
- Vault API, Direct Data API, Microsoft Office integration
- Official website
- veeva.com
Veeva is a suite of cloud-based applications for the life sciences industry. The platform includes solutions for clinical trial operations, regulatory submissions, safety monitoring, and quality management. It is built on the Vault Platform, which manages data, content, and AI agents.
This software is designed for pharmaceutical, biotechnology, and medical device companies, as well as research sites. It supports tasks such as managing investigator site files electronically, authoring regulatory documents, and managing commercial CRM activities.
Buyers should consider that the platform is specialized for regulated industries. Because it offers various modules, users should confirm which specific clouds—such as Clinical, Quality, or Safety—align with their operational needs.
Key Features
A centralized cloud environment for managing industry-specific data, content, and AI agents.
Tools for clinical trials, including eTMF for inspection readiness and CTMS for trial management.
Applications to plan, author, review, and approve regulatory documents and track global registrations.
Supports quality processes including GxP document control, QMS, and validation management.
Agentic AI integrated into the Vault Platform to provide industry-specific assistance and support workflows.
Solutions for research sites to digitize study binders and track patient activity.
Use Cases
Using CTMS and eTMF to track patient activity and maintain documentation.
Planning and authoring regulatory documents to manage submissions to health authorities.
Transitioning from paper-based or fragmented systems to a unified quality management system (QMS).
Managing the intake and processing of adverse events through a safety platform.
Digitizing study binders using eISF to support remote monitoring.
Best For
Integrations
Pricing
SiteVault is free for research sites with up to 20 active studies. Pricing for larger sites is tiered. Buyers should confirm current pricing on the vendor website.
FAQ
Veeva is designed for the global life sciences industry, including pharmaceutical, biotechnology, and MedTech companies, and clinical research sites.
SiteVault is free for research sites with up to 20 active studies; larger sites use tiered pricing.
Veeva maintains certifications for ISO 27001, ISO 27018, and SOC 2 Type II, and is ISO 9001 certified for quality management.
Source category: Healthcare
Source subcategory: Compliance Management
