Healthcare
DocuHub + Veeva
Integrate DocuHub with Veeva Vault for 21 CFR Part 11 compliant document signing in life sciences. Manage clinical trial documents, regulatory submissions, and quality records with validated signing.
DocuHub
EnterpriseHealthcare
What You Can Do with DocuHub + Veeva
Life sciences compliance signing
21 CFR Part 11 Compliance
Validated electronic signatures meet FDA 21 CFR Part 11 requirements for pharmaceutical documents.
Vault Integration
Import documents from Veeva Vault for signing and store executed copies back with full metadata.
Audit Trail
Tamper-evident audit trails meet GxP requirements for clinical, quality, and regulatory documents.
Multi-Signature Workflows
Route documents through complex approval chains — author, reviewer, approver — required in regulated environments.
How It Works
Connect Veeva to DocuHub in just a few steps.
1
Validate the Integration
Complete IQ/OQ/PQ validation of the DocuHub-Veeva integration per GxP requirements.
2
Configure signing workflows
Map Veeva Vault document lifecycle states to DocuHub signing workflows with role-based routing.
3
Sign compliantly
Documents are signed with validated electronic signatures; audit trails meet regulatory requirements.
Real-World Use Cases
See how teams use DocuHub + Veeva to streamline their workflows.
Clinical Trial Protocols
Sponsors route clinical trial protocols through investigator review and signature using validated DocuHub signing within Veeva Vault.
Quality SOPs
Quality teams manage SOP lifecycle with DocuHub signing for authoring, review, and approval workflows.
Regulatory Submissions
Regulatory affairs teams sign and certify submission documents with compliant electronic signatures.
Get Started with DocuHub + Veeva
Connect Veeva and supercharge your document workflows. Free to start — no credit card required.
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