GLP Training

Good Laboratory Practices (GLP) training — OECD principles, study director responsibilities, raw data discipline, archives, and audit fundamentals.

What is GLP Training?

This programme makes Good Laboratory Practices (GLP) a daily working framework, not a textbook concept. You learn what an OECD-compliant non-clinical safety study actually demands — from study-director responsibilities to archive integrity.

What you will learn

OECD Principles of GLP — scope, applicability, and intent
Roles — Sponsor, Study Director, Test Facility Management, QA Unit
Test article and reference item handling and accountability
Raw data discipline — original observations, corrections, ALCOA+
Standard Operating Procedures and SOP control under GLP
Archives and study-record retention

Who this is for

Students and early-career professionals from pharmacy, life sciences, toxicology, biotechnology, and chemistry targeting non-clinical CRO, GLP-laboratory, or safety-study roles.

What you take away

NTHRYS training certificate detailing GLP scope
A practical understanding of how GLP is operated, not just defined
Documentation literacy that GLP CROs immediately recognise
A focused profile for non-clinical / GLP-lab careers

Pick the field below to see specific GLP training options.

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