Understanding GxP

This Understanding GxP Fundamentals course provides a comprehensive introduction to Good Practice (GxP) regulations and compliance requirements applicable across the pharmaceutical, biotechnology, medical device, healthcare, and life sciences industries. The course covers key concepts such as GxP principles, Good Documentation Practices (GDP), data integrity, quality management systems, risk management, validation, change control, deviations, CAPA, and regulatory compliance expectations. Designed for students, freshers, and working professionals, this self-paced e-learning program helps learners develop a strong foundation in GxP requirements, regulatory standards, inspection readiness, and quality culture essential for working in regulated environments.