AI TOOL PROFILE
Veeva: Cloud Software for Life Sciences
- Healthcare
- Compliance Management
- 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.
At a glance
- Best for
- Pharmaceutical companies, Biotechnology organizations, MedTech companies, Clinical research sites, Life sciences R&D teams
- 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
- Visit Veeva official website
How AI is used
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
Veeva Vault Platform
A centralized cloud environment for managing industry-specific data, content, and AI agents.
Clinical Solutions
Tools for clinical trials, including eTMF for inspection readiness and CTMS for trial management.
Regulatory Solutions (RIM)
Applications to plan, author, review, and approve regulatory documents and track global registrations.
Quality Cloud
Supports quality processes including GxP document control, QMS, and validation management.
Veeva AI
Agentic AI integrated into the Vault Platform to provide industry-specific assistance and support workflows.
SiteVault
Solutions for research sites to digitize study binders and track patient activity.
Use Cases
Clinical Trial Management
Using CTMS and eTMF to track patient activity and maintain documentation.
Regulatory Submission Planning
Planning and authoring regulatory documents to manage submissions to health authorities.
Quality Process Centralization
Transitioning from paper-based or fragmented systems to a unified quality management system (QMS).
Pharmacovigilance
Managing the intake and processing of adverse events through a safety platform.
Digital Investigator Site Files
Digitizing study binders using eISF to support remote monitoring.
Integrations
- Vault API
- Direct Data API
- Microsoft Office integration
FAQ
Who is Veeva designed for?
- Veeva is designed for the global life sciences industry, including pharmaceutical, biotechnology, and MedTech companies, and clinical research sites.
Does Veeva offer a free plan?
- SiteVault is free for research sites with up to 20 active studies; larger sites use tiered pricing.
What security certifications does Veeva have?
- 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
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