CentraLabS is a leading service provider for specimen archival management and for long-term storage. CentraLabS in-house 24-hour surveillance and computerized tolerance alarm systems maintain constant temperatures and ensures sample integrity.

CentraLabS provide the characterization and assessment of stability of pharmaceutical and biotechnology products via Good Manufacturing Process (GMP) / International Conference on Harmonization (ICH) compliant resources and world-class expertise. This cost-effective service provides comprehensive and responsive services reducing the pressure on your own resources, fulfilling your CMC requirements for the testing of active substances, formulations and delivery systems.

CentraLabS Qualified Person (QP) Services, provides advice to the sponsors in support for human clinical trial supplies via the monitoring of in-house GMP manufacturing activities for Investigational Medicinal Products (IMPs).