Why Audit Readiness Depends on a Strong Quality Management System in Pharmaceutical Manufacturing In today’s highly regulated pharmaceutical environment, audit readiness is no longer an annual exercise but an ongoing state of preparedness. Regulatory bodies such as the FDA, EMA, and other global agencies expect pharmaceutical companies to demonstrate complete control over their processes, data, and product quality at any given time. A quality management system in pharmaceutical manufacturing ensures that organizations maintain this level of vigilance. By providing structured documentation, traceability, and automated workflows, the QMS eliminates audit-related risks and establishes a culture of continuous compliance. For leaders in life sciences, audit readiness is both a regulatory requirement and a competitive advantage that builds stakeholder trust.
The Role of a Quality Management System in Pharmaceutical Manufacturing for Audit Readiness 공개
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