Veeva Auditor Guide Audit Guide
Veeva Auditor Guide Audit Guide
  • Audit Overview
  • Document List
  • Veeva Product Help Pages
  • ComplianceDocs
    • Welcome
    • About Veeva
    • About Veeva Products
    • What is Vault?
    • Audit Overview
    • ComplianceDocs & Customer FAQ
    • Quality Management System
    • Audit & Inspection Management
    • Change Management
    • CAPA
    • Management Review
    • Record Management
    • Risk Management
    • Training Management
    • Product Lifecycle
    • Software Development
    • Software Testing (SQA)
    • Release Management
    • Computer System Validation
    • Product Support
    • Technical Operations
    • Business Continuity (BC) /Disaster Recovery (DR)
    • Information Security
    • Data Privacy
    • Veeva RTSM
    • Veeva eCOA
    • Veeva CDMS
    • Veeva SiteVault
    • Document List (Policies/SOPs/Work Instructions)
    • Require a Quality Agreement?
    • Certificates/Regulatory Assessments
    • Pre-Filled Industry Assessments
    • Article List

Certificates / Regulatory Assessments

Certificates

Veeva’s Certificates can be found here

Downloadable Certificates:

ISO 9001 Certificate

ISO 27001/27017/27018 Certificate

ISO 14001 Certificate

Regulatory Assessments

Please see below a selection of Regulatory Assessments. A full list of assessments can be found here: Regulatory Assessments.

  • FDA 21 CFR Part 11 Compliance Assessment
  • EU Annex 11 Compliance Assessment
  • Japan ERES Compliance Assessment
  • Detailed ERES Trace Assessment – Vault
  • MyVeeva for Patients Compliance Trace
  • Network MDM Regulatory Assessment
  • Commercial Products – Regulatory Assessment
  • Digital Trails Platform – Regulatory Assessment
  • Vault Data Integrity Controls Assessment
  • HIPAA Security Standard Compliance Assessment
  • EMA GCP Compliance Response
  • GLP Principles Compliance Assessment
  • MFDS KGMP Data Integrity Assessment
  • AAMI TIR 45 – Veeva SDLC Assessment
  • EMA/INS/GMP/778430/2022 Annex 11 Revision Assessment
  • EMA / INS / GCP / 112288 / 2023 Guideline Assessment
  • ICH E6(R3) GCP Draft Assessment
  • Sites & Patients - Regulatory Assessment
This website is intended for informational purposes only and does not form part of any contract, scope of work, or quality agreement. This website is not a quality record or a commitment to deliver any specific service or deliverable. It is designed to provide a summary of Veeva's process areas to support customer audits. For any queries, please contact your assigned Veeva audit team, or email audits@veeva.com.

©2025 Veeva Systems Inc. All rights reserved.
Page last updated: Aug 20, 2025