Tag: CAPA

The Strategic Role of Quality Management System in Pharmaceutical Manufacturing Strengthening Regulatory Adherence In the pharmaceutical industry, compliance with Good Manufacturing Practices (GMP) and FDA regulations is non-negotiable. A quality management system in pharmaceutical manufacturing provides a structured approach to managing processes, documentation, and product quality. By integrating quality management system principles into daily operations, […]

Strengthening Audit Readiness Through CAPA in Pharmaceutical Operations Regulatory audits in the pharmaceutical industry are becoming more rigorous as global agencies demand strict adherence to Good Manufacturing Practices (GMP), data integrity, and quality management requirements. To achieve consistent success in these audits, organizations must go beyond surface-level compliance and embrace a proactive framework for managing […]