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Veeva eTMF

Paid

Secure, cloud‑based electronic trial master file for regulated pharmaceutical studies.

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4.6 Editor Rating
Vetted Score
4.6 / 5.0

Earns a high score for its robust compliance features, seamless cloud access, and strong integration with other Veeva applications, though pricing is premium.

Key Features
Regulatory‑Compliant Document Management

Centralized storage, version control, and audit trails that meet FDA 21 CFR Part 11 and EMA requirements.

Role‑Based Access & Permissions

Granular security settings ensure users see only the data relevant to their responsibilities.

Integrated Workflow Automation

Automated routing, review, and approval processes accelerate study timelines and reduce manual errors.

Frequently Asked Questions

No, Veeva eTMF is delivered exclusively as a cloud‑based SaaS platform.

It uses a subscription model with tiered per‑user pricing; exact costs are provided via custom enterprise quotes.

Yes, it offers APIs and pre‑built connectors for popular eClinical and data‑management solutions.
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Specifications
Pricing Model Subscription‑based SaaS with tiered user pricing; custom enterprise quotes typically start around $30 USD per user per month and can scale up to $150 USD for advanced modules.
Supported Platforms
Web browsers (Chrome, Firefox, Edge, Safari)iOSAndroid
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