VigiloIQ for Life Sciences

Life Sciences Contract Management Platform

VigiloIQ equips legal, clinical operations, and procurement teams with a centralized infrastructure for managing Clinical Trial Agreements (CTAs), vendor contracts, and IP licensing obligations.

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Contract Oversight for Biotech & Pharma

  • ✓ Clinical Trial Management: Centralizes site agreements, investigator contracts, and budget amendments for global studies.
  • ✓ Vendor Compliance: Monitors CRO and supplier obligations against quality agreements and regulatory requirements.
  • ✓ IP & Licensing Tracking: Tracks royalty milestones, patent expirations, and collaborative research obligations.
  • ✓ Audit Readiness: Maintains an immutable audit trail of approvals and version history for regulatory inspection.
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Compliance

FDA & EMA audit support

Operational Impact
40%
Faster CTA execution
|
100%
Visibility into CRO obligations
|
Verified
Audit trail integrity

How VigiloIQ Supports Life Sciences

VigiloIQ provides the operational capabilities for clinical site contracting, vendor quality management, and regulatory audit preparation.

Clinical Agreement Drafting

Accelerates the generation of Clinical Trial Agreements (CTAs) and site budgets using templates approved by legal and clinical leadership.

Vendor Quality Agreements

Centralizes quality agreements with CROs, labs, and manufacturers to track adherence to performance metrics and regulatory standards defined in the contract.

Milestone & Obligation Tracking

Monitors critical dates for regulatory filings, safety reporting, and patient enrollment milestones to prevent study delays.

Regulatory Intelligence Q&A

Enables clinical teams to query contract documents via natural language to instantly verify reporting responsibilities and data privacy clauses.

R&D Procurement Support

Deploys AI agents to assist research teams with supplier contracting, ensuring lab equipment and service agreements align with procurement policy.

Global Template Standardization

Centralizes approved legal templates to ensure consistent liability, IP ownership, and indemnification terms across all clinical and commercial agreements.

Centralized Oversight for Clinical Agreements

Evaluate VigiloIQ as the system of record for clinical trial contracting, vendor quality management, and regulatory audit support.

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