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Data flow: Veeva Vault ? Adobe Experience Manager Sites
Marketing and medical teams can author and approve regulated product claims, label language, and supporting references in Veeva Vault, then publish only approved content to Adobe Experience Manager Sites for use on public product pages, disease education pages, and campaign landing pages. This ensures web content stays aligned with the latest compliant source material while reducing manual re-entry and review risk.
Business value: Faster web publishing, fewer compliance errors, and a single controlled source for regulated content.
Data flow: Veeva Vault ? Adobe Experience Manager Sites
Life sciences organizations often manage multilingual product labels, indications, and safety statements in Veeva Vault. These approved translations can be synchronized into Adobe Experience Manager Sites to power localized websites across regions, ensuring each market displays the correct language version, approved claims, and country-specific disclaimers.
Business value: Consistent global messaging, reduced localization effort, and improved speed to market for regional launches.
Data flow: Adobe Experience Manager Sites ? Veeva Vault ? Adobe Experience Manager Sites
Content teams can draft or update web pages in Adobe Experience Manager Sites, then route the content or supporting assets into Veeva Vault for medical legal regulatory review and approval. Once approved, the final version is returned to Adobe Experience Manager Sites for publication. This creates a controlled workflow for high-risk content such as product claims, safety information, and indication statements.
Business value: Stronger governance, auditable approvals, and reduced review cycle friction between marketing and compliance teams.
Data flow: Veeva Vault ? Adobe Experience Manager Sites
Promotional banners, product visuals, approved PDFs, and campaign copy stored in Veeva Vault can be pushed into Adobe Experience Manager Sites as reusable content components or linked assets. Web teams can then assemble campaign pages without manually handling regulated files, while maintaining traceability to the approved source.
Business value: Reusable approved assets, lower content production overhead, and fewer version control issues.
Data flow: Veeva Vault ? Adobe Experience Manager Sites
Clinical operations teams can manage approved study descriptions, eligibility criteria, site contact details, and patient-facing trial materials in Veeva Vault. Adobe Experience Manager Sites can then publish these details on recruitment pages or study portals, ensuring that only current, approved trial information is displayed to patients, investigators, and site staff.
Business value: Better patient engagement, reduced risk of outdated trial information, and improved operational control over study communications.
Data flow: Bi-directional
When a product claim, indication, or campaign asset is retired in Veeva Vault, the integration can trigger corresponding removal, unpublishing, or archival actions in Adobe Experience Manager Sites. This prevents expired or noncompliant content from remaining live on digital properties and supports consistent retention policies across both systems.
Business value: Reduced compliance exposure, cleaner content lifecycle management, and less manual cleanup work for web teams.
Data flow: Veeva Vault ? Adobe Experience Manager Sites
Veeva Vault can serve as the system of record for claim substantiation, reference documents, and approved supporting materials. Adobe Experience Manager Sites can surface these references on product pages, downloadable resource sections, or medical information pages, giving users access to the approved evidence behind published claims.
Business value: Improved transparency, easier compliance validation, and stronger support for regulated digital content.
Data flow: Bi-directional
For product launches, label changes, or safety updates, Veeva Vault can manage the regulated approval process while Adobe Experience Manager Sites manages the customer-facing experience. Status updates, approval outcomes, and content version references can be synchronized so marketing, regulatory, and digital teams work from the same launch timeline and content state.
Business value: Better coordination across functions, fewer launch delays, and a more reliable end-to-end content operating model.