Good Laboratory Practice (GLP) Compliance Program

$ 150

In stock

Course Description

This program provides comprehensive training in Good Laboratory Practice standards as applied in non-clinical safety studies. Participants learn the organizational processes and conditions required to ensure the quality, integrity, and traceability of non-clinical research data in compliance with OECD GLP Principles.

Program Modules

• Introduction to GLP: OECD Principles, History & Regulatory Basis
• Test Facility Organization: Management, Quality Assurance Unit & Roles
• Standard Operating Procedures: Writing, Approval & Management
• Study Plans, Protocols & Experimental Design in GLP Studies
• Test Article & Reference Substance Characterization & Accountability
• Equipment Qualification, Calibration & Maintenance Records
• Data Integrity: ALCOA+ Principles, Raw Data Management & Archiving
• GLP Inspections, Audit Findings & Non-Compliance Management

Who Should Attend

Laboratory scientists conducting non-clinical safety studies, quality assurance officers, study directors, research managers, and regulatory affairs professionals in pharmaceutical, chemical, and contract research organizations.

Course Details

• Duration: 4 Days
• Investment: $150 per participant