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Veeva Expands Veeva Vault Regulatory Capabilities for Medical Device and Diagnostics

Organizations can unify product registrations, health authority correspondence and commitments, and submissions documents on a single cloud platform for one global authoritative source of regulatory information.

Debiopharm International SA Strengthens Compliance and Clinical Trial Oversight with Veeva Vault eTMF

4/17/18: “Veeva is helping us streamline our clinical operations,” said Christian A. Aeschlimann, director of clinical operations at Debiopharm. “Veeva Vault eTMF will help us maintain an always-accurate, up-to-date TMF and align with external partners by working in the same system.”