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Data flow: SFTP ? Veeva Vault
External agencies, contract manufacturers, or regional affiliates can drop approved source files into a secure SFTP folder for automated ingestion into Veeva Vault. Typical content includes product labels, clinical study documents, artwork files, or submission-ready PDFs. Veeva Vault then routes the content through controlled review and approval workflows, ensuring regulated materials enter the system with traceability and compliance controls.
Business value: Reduces manual email-based file handling, shortens intake cycles, and improves auditability for regulated content onboarding.
Data flow: Veeva Vault ? SFTP
Once documents are approved in Veeva Vault, the final controlled versions can be exported to an SFTP location for downstream consumption by print vendors, localization agencies, distributors, or regulatory service providers. This is useful for approved product inserts, packaging artwork, training materials, and submission packages that must be shared securely outside the Veeva environment.
Business value: Ensures partners receive only approved, version-controlled files while maintaining secure transfer and delivery logs.
Data flow: Bi-directional
Clinical operations teams can use SFTP as a secure exchange channel for study documents such as investigator brochures, site activation packets, monitoring reports, and signed forms. Veeva Vault manages the controlled document lifecycle, while SFTP supports encrypted transfer to and from contract research organizations and trial sites that require a simple, standards-based file exchange method.
Business value: Supports faster study startup and document exchange while preserving compliance, access control, and transfer traceability.
Data flow: SFTP ? Veeva Vault, and Veeva Vault ? SFTP
Marketing agencies can deliver high-resolution images, videos, and campaign files through SFTP into Veeva Vault for medical legal regulatory review. After approval, the final assets can be exported back to SFTP for distribution to regional marketing teams, digital asset repositories, or approved production vendors. This pattern is especially useful for multilingual and market-specific promotional content.
Business value: Speeds review cycles, centralizes compliance control, and reduces the risk of using unapproved promotional materials.
Data flow: Bi-directional
Regulatory affairs teams can assemble submission content in Veeva Vault and exchange submission-ready packages with external publishing vendors or regulatory consultants via SFTP. Vendors can return validation reports, publishing outputs, or corrected files through the same secure channel. Veeva Vault remains the system of record for document status, versioning, and approval history.
Business value: Improves submission coordination, reduces rework, and creates a secure, auditable handoff process with external regulatory partners.
Data flow: Veeva Vault ? SFTP
When product information, labeling text, or approved claims are updated in Veeva Vault, the final files can be published to SFTP for regional affiliates, distributors, or local compliance teams. This supports controlled rollout of updated product information across markets, especially where downstream systems cannot connect directly to Veeva Vault.
Business value: Enables consistent global content distribution and reduces delays in local market adoption of approved updates.
Data flow: Veeva Vault ? SFTP
Organizations can export archived regulated documents from Veeva Vault to an encrypted SFTP repository for long-term retention, backup, or disaster recovery purposes. This is useful for maintaining offline copies of critical quality documents, clinical records, and submission materials in line with retention policies and business continuity requirements.
Business value: Strengthens resilience, supports retention compliance, and provides an additional secure copy of critical regulated content.