Our GLP service capabilities
End-to-end GLP audit capabilities that support compliant laboratory operations, align with regulatory expectations and maintain data credibility across non-clinical studies.
GLP compliance strategy and implementation
Practical frameworks aligned to regulatory expectations and the realities of non-clinical laboratory operations.
Laboratory quality management systems (QMS)
GLP-compliant QMS design and enhancement that supports study conduct, documentation control and traceability.
Study conduct and data integrity controls
Risk-based controls to ensure reliable data generation, review and reporting.
Audit readiness and regulatory inspection support
Hands-on preparation, inspection support and post-inspection remediation.
Vendor, assay and method oversight
Oversight models that maintain GLP compliance across internal and outsourced activities.
Interim QA and laboratory compliance leadership
Flexible, embedded expertise to strengthen GLP oversight during periods of change or increased demand.
