Pharma Regulatory & Quality Compliance

Description

To equip participants with an in-depth understanding of global pharmaceutical regulations, GxP compliance, documentation standards, and regulatory submission processes, ensuring adherence to FDA, EMA, CDSCO, WHO, and other guidelines.

Master global pharma regulations, GMP standards, and audit readiness in one comprehensive program.

This industry-focused course is designed to train professionals in the pharmaceutical, biotech, and healthcare sectors on the critical aspects of regulatory affairs, quality assurance, and compliance. Whether you’re preparing for global audits or submitting regulatory dossiers, this course gives you the tools, frameworks, and confidence to meet international compliance standards.