Healthcare
DocuHub + IQVIA
Connect DocuHub to IQVIA platforms for clinical trial document management, site agreements, and regulatory compliance across pharmaceutical and contract research organizations.
DocuHub
EnterpriseHealthcare
What You Can Do with DocuHub + IQVIA
Pharma and CRO document management
Site Agreement Signing
Send clinical trial site agreements, budgets, and informed consent forms for electronic signature.
TMF Integration
Signed documents are filed in the Trial Master File (TMF) with proper indexing and metadata.
Multi-Country Support
Support for multi-country clinical trials with locale-specific documents and signing requirements.
Regulatory Compliance
Signing workflows meet ICH-GCP, FDA, and EMA requirements for electronic signatures on clinical documents.
How It Works
Connect IQVIA to DocuHub in just a few steps.
1
Connect IQVIA
Configure DocuHub integration with your IQVIA platform instance for clinical document workflows.
2
Map document types
Link clinical document types — protocols, ICFs, site agreements — to DocuHub templates and signing workflows.
3
Execute and file
Documents are signed electronically; executed copies are filed in the TMF with regulatory-compliant audit trails.
Real-World Use Cases
See how teams use DocuHub + IQVIA to streamline their workflows.
Global Clinical Trials
CROs managing multi-country trials send locale-specific informed consent forms to sites in 30+ countries for electronic signature.
Site Activation
Sponsors send site activation packages — agreements, budgets, insurance certificates — for investigator signature.
Safety Reporting
Safety teams route expedited safety reports for medical review and sign-off with compliant electronic signatures.
Get Started with DocuHub + IQVIA
Connect IQVIA and supercharge your document workflows. Free to start — no credit card required.
Get Started Free