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AI-powered content management software for life sciences

Vodori's Regulated Content Intelligence Platform™ brings MLR review, claims management, workflow, and distribution together in one governed system. AI is built in to help teams catch issues earlier, approve faster, and reuse what they've learned, while humans stay in charge of every decision.

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Trusted by over 100 life science teams globally

 

Why do life science teams choose Vodori?

A unique customer success program built of industry and process experts committed to your success. Learn more about what makes our program different and the numerous ways we deliver value to our customers outside of great software. 

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How does Vodori meet life sciences compliance and security requirements?

Vodori is 21 CFR Part 11 and EU Annex 11 compliant, GxP validated, and audited annually for SOC 2 Type 2. Every review action is captured in a complete audit trail with enforced electronic signatures, so quality and regulatory teams can produce inspection-ready records for FDA, EMA and EU MDR audits in hours instead of days.

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Audit trails and e-signatures

Every comment, vote, change and approval is time-stamped and attributed to a named user. Enforced electronic signatures meet 21 CFR Part 11 and Annex 11 requirements.
Complete version history

Every version of every asset is kept with its review record, so you can show exactly what was approved, by whom, and when.
Validated releases

Vodori pre-validates each release and provides a validation package, reducing work for your quality team.
Enterprise-grade security

Annual SOC 2 Type 2 audit, ISO 27001, and GDPR compliance.
Single Sign On

SSO connects Vodori to your identity provider, so IT manages access with the same policies it uses across the business.
Governed AI

Vodori's AI findings are advisory and recorded; AI never approves, rejects or determines compliance. Tenant isolation and zero-retention endpoints keep your content private, and customer data is never used to train AI models.
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How does Vodori fit into your commercial technology ecosystem?

Don’t settle for mediocre systems. With Vodori, you can build your ideal commercial ecosystem by connecting best-in-class systems such as Salesforce, IQVIA OCE, Seismic, and more.

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Frequently Asked Questions

What is a Regulated Content Intelligence Platform™?

A Regulated Content Intelligence Platform (RCIP) combines a system of record for governed knowledge (approved claims, scientific evidence, references, policies, and review history) with an embedded intelligence layer that applies that knowledge across authoring, review, approval, and distribution. Vodori introduced the category in 2026, starting with Content Preflight.

What is AI-powered MLR review?

AI-powered MLR review uses artificial intelligence to help life sciences teams prepare, review, approve, and manage promotional content more efficiently. Rather than replacing medical, legal, and regulatory reviewers, AI helps identify patterns, surface issues earlier, reduce preventable work, create efficiencies, and support better decision-making throughout the content lifecycle.

In regulated environments, AI is most effective when used to support content preparation, claims management, workflow efficiency, and operational decision-making. Human reviewers remain responsible for evaluating evidence, context, risk, and compliance requirements before content is approved.

Vodori embeds AI directly into our platform, helping teams improve content quality and reduce operational friction while maintaining governance, auditability, and human oversight.

How can AI improve promotional review?

AI can improve promotional review by helping teams identify issues earlier, reduce avoidable rework, and improve the quality of content entering review. Common use cases include detecting content quality issues, harvesting and managing claims, identifying inconsistencies, and helping reviewers focus on higher-value scientific, medical, and regulatory considerations.

As content volumes continue to grow, AI can also help organizations scale review operations without increasing reviewer burden. By identifying potential issues before formal review begins, teams can reduce recirculation, shorten review cycles, and make more efficient use of reviewer expertise.

The greatest value comes when AI is embedded directly into the promotional review system rather than operating as a standalone productivity tool outside the review process.

Does AI replace MLR reviewers?

No. AI cannot replace the scientific, medical, legal, and regulatory judgment required during MLR review.

AI is effective at identifying patterns, surfacing potential issues, and automating repetitive tasks, but it cannot evaluate clinical context, determine regulatory appropriateness, assess risk, or make approval decisions. Those responsibilities require human expertise and accountability.

Vodori is an AI-powered content review platform designed to support reviewers, not replace them. AI surfaces quality, claims, and governance signals that may require attention, while human reviewers remain responsible for evaluating content, making decisions, and approving materials.

How does Vodori compare to Veeva?

Veeva Vault PromoMats and Vodori are the only two purpose-built MLR (medical, legal, regulatory) review platforms on the market. Veeva Vault PromoMats is built for top-20 pharma organizations already standardized on the Veeva ecosystem. Vodori is built for life sciences teams that prioritize faster implementation (typically 4 to 6 weeks vs. 16 to 24+ for Veeva), transparent pricing, an open ecosystem, and the only native Salesforce AppExchange MLR partnership. Most pharma marketing organizations outside top-20 pharma find Vodori delivers a better fit on speed, total cost of ownership, and day-to-day usability.

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