Tag: GMP non-compliance

Preventing Cross-Contamination in Pharma

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Preventing Cross-Contamination in Pharma Effective Strategies for Preventing Cross-Contamination in Pharmaceutical Manufacturing Introduction: The Criticality of Cross-Contamination Prevention Cross-contamination poses significant risks in pharmaceutical manufacturing, potentially compromising product quality, patient safety, and regulatory compliance. In facilities adhering to Good Manufacturing Practices (GMP), preventing cross-contamination is a priority to maintain product integrity and comply with stringent…

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Preventing Cross-Contamination in Pharma

Continuous Improvement in GMP

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Continuous Improvement in GMP How to Achieve Continuous Improvement in GMP Pharmaceutical Manufacturing Introduction: The Importance of Continuous Improvement in GMP Good Manufacturing Practices (GMP) are the foundation of quality and compliance in pharmaceutical manufacturing. However, compliance is not a one-time achievement but a continuous process that evolves with technological advancements, regulatory updates, and operational…

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Continuous Improvement in GMP

What is Total Quality Management (TQM) and How Does It Apply to GMP?

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What is Total Quality Management (TQM) and How Does It Apply to GMP? Understanding Total Quality Management and Its Application in GMP An Overview of Total Quality Management (TQM) Total Quality Management (TQM) is a structured approach to enhancing the quality and consistency of products, services, and processes within an organization. Rooted in a philosophy…

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Total Quality Management (TQM) in GMP