Good Laboratory Practice (GLP)
Our GLP team has the experience and capability to conduct audits of all types including: facilities; process data; study specific data and reports against GLP requirements. We audit central laboratories and bio-analytical laboratories for routine and specialized analysis against both GLP and GCP regulations.
compliance.
Safety.
Integrity.
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.
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.
Blog
In the ever-evolving landscape of clinical trials, the recent update to the ICH E6(R3) Good Clinical Practice (GCP) guidelines marks a pivotal shift in how sponsors and service providers manage and oversee these complex processes.
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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