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IQVIA Labmatrix

by IQVIAiqvia.com
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OVERVIEW

A comprehensive, cloud-based system for clinical trial sample and consent management, utilized in over 1,000 trials to streamline operations and ensure regulatory compliance.

IQVIA Labmatrix is an industry-leading, highly configurable, cloud-based solution for Clinical Trial Sample and Consent Tracking (CTST) and Next Generation Biobanking . Developed by BioFortis (acquired by IQVIA Laboratories), it is designed to streamline clinical trial operations, maximize the value of biospecimens, and ensure regulatory compliance . The system is utilized in over 1,000 trials, providing a sample-centric view across the complex ecosystem of sites, labs, vendors, and biobanks .

Key Capabilities & Features

  • Sample and Consent Tracking: Provides clear visibility into study subjects, samples, and consent, ensuring sample usage corresponds with patient consent for both in-study and future-use . The system offers robust tracking of consent parameters at study, country, site, and patient levels .
  • Compliance & Audit: Features detailed chain of custody tracking and a paperless workflow within a 21 CFR Part 11-compliant system, significantly reducing operational and regulatory risks .
  • Automation & Integration: Offers automated reconciliation of planned versus actual biospecimen collection and shipment, scalable data standardization, and integration with third-party equipment, middleware, and data sources like Microsoft Azure message bus .
  • Data & Analytics: Includes configurable dashboards, robust reporting, and integration with Qiagram, a patented graphical query and analysis tool, for advanced data interrogation and visualization . The platform is 100% user-configurable for search and reporting on all data points .
  • Biobanking: Supports Next Generation Biobanking by functioning as a knowledge hub that harmonizes biospecimens with clinical and molecular data to drive precision medicine research .

Target Users and Benefits

Labmatrix is primarily targeted at top pharmaceutical companies, biotech firms, and academic institutions involved in clinical trials and biobanking . It helps reduce the risk of sample logistics becoming a bottleneck in clinical trial execution, enables earlier discovery of biospecimen problems, and optimizes sample storage capacity .

RATING & STATS

Customers
1,000+
Founded
2002

KEY FEATURES

  • Clinical Trial Sample and Consent Tracking (CTST)
  • Detailed Chain of Custody Tracking
  • Automated Biospecimen Reconciliation
  • Computable Patient Consent Management
  • Configurable Dashboards and Reporting
  • Virtual Biorepository and Storage Management
  • Scalable Data Standardization and Integration
  • Workflow Management for Analysis/Destruction Requests
  • Single Sign-On (SSO) Support

PRICING

Model: enterprise
Pricing is not publicly disclosed and is structured for enterprise-level clinical trial and biobanking operations. Contact IQVIA for a quote.

TECHNICAL DETAILS

Deployment: cloud
Platforms: web
🔌 API Available

USE CASES

Clinical Trial Sample ManagementBiobanking OperationsBiospecimen and Consent TrackingPrecision Medicine ResearchRegulatory Compliance and Audit Readiness

INTEGRATIONS

Qiagram (IQVIA's graphical query tool)Third-party laboratory equipment and middlewareMicrosoft Azure message buseClinical data sources

COMPLIANCE & SECURITY

Compliance:
FDA 21 CFR Part 11
Security Features:
  • 🔒SSO
  • 🔒Fine-grained Access Controls
  • 🔒Encryption

SUPPORT & IMPLEMENTATION

Support: email, phone, dedicated support
Implementation Time: 1-3 months
Target Company Size: medium, enterprise
TRAINING AVAILABLE

PROS & CONS

✓ Pros:
  • +Comprehensive sample and consent tracking across the entire clinical trial ecosystem
  • +Reduces operational and compliance risks (e.g., 21 CFR Part 11, consent alignment)
  • +Scalable data standardization and integration without custom programming
  • +Enables earlier discovery and resolution of biospecimen problems
  • +Supports Next Generation Biobanking and precision medicine research
✗ Cons:
  • -Pricing and implementation details are not publicly transparent
  • -No public third-party reviews or ratings available

ABOUT IQVIA

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