Home | Connectors | Veeva Vault | Veeva Vault - OpenText Active Community - Trading Grid Integration and Automation
Direction: Veeva Vault ? OpenText Active Community - Trading Grid
Life sciences companies can publish approved regulatory, quality, or product documents from Veeva Vault into Trading Grid communities for controlled sharing with contract manufacturers, distributors, and other external partners. This supports secure exchange of SOPs, specifications, certificates, and approved labeling content while preserving version control and auditability.
Business value: Reduces manual email-based document sharing, improves partner access to current approved content, and lowers compliance risk.
Direction: Bi-directional
When a trading partner reports a quality deviation, packaging discrepancy, or document mismatch in Trading Grid, the issue can be routed into Veeva Vault quality or document workflows for review, investigation, and approval. Status updates and resolution notes can then be sent back to the partner community.
Business value: Speeds exception handling, improves traceability, and creates a closed-loop process between internal quality teams and external partners.
Direction: Veeva Vault ? OpenText Active Community - Trading Grid
Marketing, medical, and regulatory teams can approve product claims, promotional assets, and multilingual label content in Veeva Vault, then distribute the finalized materials to external agencies, distributors, or regional partners through Trading Grid. Partners receive only approved content and can access the latest version in a shared community workspace.
Business value: Ensures consistent brand and compliance messaging across the partner network while reducing rework and outdated content usage.
Direction: OpenText Active Community - Trading Grid ? Veeva Vault
Trading Grid can be used to collect partner feedback on packaging artwork, regional labeling requirements, or submission-related documents. Comments, redlines, and supporting files can be transferred into Veeva Vault for formal review and approval by regulatory, legal, or quality teams.
Business value: Centralizes external input into a controlled workflow and shortens cycle times for content updates and market readiness.
Direction: Bi-directional
For regulatory submissions involving CROs, CMOs, or local affiliates, Veeva Vault can manage the authoritative submission package while Trading Grid serves as the collaboration layer for exchanging supporting documents, clarifications, and missing artifacts. Updates from partners can be ingested into Vault, and approved submission materials can be shared back out through the community.
Business value: Improves coordination across distributed submission teams and reduces delays caused by fragmented document exchange.
Direction: Bi-directional
Packaging artwork, carton copy, and label updates approved in Veeva Vault can be shared with packaging suppliers and print vendors through Trading Grid. Suppliers can return proofs, corrections, or production confirmations through the same community, with final approved versions retained in Vault.
Business value: Reduces packaging errors, improves supplier accountability, and supports faster change implementation across markets.
Direction: Bi-directional
Clinical operations teams can use Veeva Vault to manage controlled trial documents such as investigator brochures, site instructions, and essential documents, then share approved materials with external study partners through Trading Grid. Partners can upload acknowledgements, requested updates, or supporting files back into the shared workflow.
Business value: Enhances collaboration with CROs and sites while maintaining inspection-ready document control.
Direction: OpenText Active Community - Trading Grid ? Veeva Vault
Key partner communications, approvals, and document exchange records from Trading Grid can be archived in Veeva Vault as part of the regulated content record. This creates a complete history of what was shared, when it was approved, and who acknowledged it.
Business value: Strengthens audit readiness, supports regulatory inspections, and provides a defensible record of external collaboration.