Pharmaceutical GLP – Corporate Training

Description

Pharmaceutical GLP – Corporate Training

This comprehensive training program is designed to equip pharmaceutical professionals with a strong foundation in Good Laboratory Practices (GLP), ensuring regulatory compliance, data integrity, and operational excellence. Key Learning Areas:

• GLP Principles & Laboratory Framework Understanding core GLP requirements, including organisation structure, personnel responsibilities, standard operating procedures (SOPs), material control, equipment management, reagents, calibration, and traceability.
• Method Validation & Sample Management: Ensuring the use of validated methods and instruments, along with proper sample handling, documentation, and maintenance of the chain of custody.
• Quality Assurance & Compliance: Implementing GLP compliance through internal audits, accurate record-keeping, systematic archiving, and maintaining report integrity.
• Safety, Environment & Ethics: Promoting safe laboratory practices, environmental responsibility, and ethical considerations, including compliance with animal study regulations where applicable.
• Handling Non-Compliance: Identifying deviations, reporting issues effectively, implementing corrective and preventive actions (CAPA), and minimising recurrence.

Note: A detailed training module and customised curriculum can be provided upon request.   https://www.youtube.com/watch?v=p1AIt-y1gzg&t=7s