Qualified independent auditing that provides assurance of compliance

Good Laboratory Practice (GLP)

Comprehensive GLP auditing for non-clinical safety studies. We verify compliance at test facilities, central labs, and bioanalytical sites to ensure data integrity.

Our GLP experts audit facilities, processes, and study data against international regulations (OECD, FDA, EPA). We provide rigorous oversight of your external vendors and internal labs, ensuring your pre-clinical data is robust and regulatory-ready. Whether for a specific study audit or a full facility inspection, we guarantee thorough compliance verification.

Request a GLP Audit

compliance.
Safety.
Integrity.

SERVICES BROCHURE
ASSURANCE AND CONFIDENCE ARE VALUES WE LIVE BY AND WE UNDERSTAND THEY UNDERPIN YOUR COMPLIANCE ACTIVITIES

Featured Resources

For a deeper dive into the ICH E6(R3) guidelines, check out our latest expert insights.

Webinar

ADAMAS Consulting’s webinar, “GCP ICH E6 R3 Unveiled: Navigating the Evolving Roles of Sponsors and CROs,” provides invaluable insights into the evolving landscape of Good Clinical Practice (GCP) guidelines.

Watch Webinar

Case Study

Our latest case study highlights how ADAMAS Consulting supported a leading pharmaceutical company in proactively identifying high-risk sites during a global Phase III oncology trial—aligning with ICH E6 (R3) guidelines.

Read Case Study

Guide

In this free guide, we break down the most critical updates to ICH E6(R3)—and provide practical, inspection-ready strategies to help you stay compliant, audit-ready, and ahead of regulatory expectations.
Download Guide
Our GcLP Services include, audits of clinical and bioanalytical laboratories that process human samples for safety parameters, biomarkers, other specialty analysis, bioequivalence etc

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