Good Laboratory Practices (GLP) for Life Sciences

Good Laboratory Practices (GLP) for Life Sciences provides a comprehensive understanding of GLP to help life sciences professionals, biotech companies, and UNH-affiliated labs ensure compliance with FDA, OECD, and WHO guidelines. This workshop is designed to equip participants with the knowledge and skills needed to maintain high-quality laboratory standards, uphold data integrity, and meet global regulatory requirements.

Workshop topics include:

• Regulatory Foundations of GLP – The role of GLP in laboratory compliance and research integrity.
• How to Navigate GLP Regulations – Practical understanding of FDA, OECD, and WHO guidelines for laboratory operations.
• Maintaining Data Integrity & Audit Preparedness – Best practices for documentation, quality assurance, and compliance monitoring.
• Steps to Establish a GLP-Compliant Laboratory – Key considerations for infrastructure, SOPs, personnel training, and risk mitigation.
• Applying GLP Principles in Real-World Scenarios – Interactive case studies, industry challenges, and mock audits.

This workshop is designed for professionals in biotech, pharmaceuticals, contract research organizations (CROs), and academic labs looking to enhance compliance, improve laboratory standards, and strengthen regulatory readiness.