End-to-end recall execution under EU GDP/GMP

This course provides a practical, real world guide to managing pharmaceutical product recalls within the EU regulatory framework. It is designed for professionals responsible for quality, compliance, and batch release who need to make defensible decisions under pressure.

Rather than focusing solely on legislation, the course emphasises how recalls are actually identified, assessed, and executed in practice, with particular attention to avoiding common regulatory and operational mistakes.

The content is aligned with expectations from the Health Products Regulatory Authority and broader EU guidance, including principles reflected by the European Medicines Agency.