Packaging and labeling control in pharmaceutical manufacturing involves systematic management, verification, and validation of packaging materials, containers, labels, and the associated processes. This ensures that all aspects of packaging and labeling comply with regulatory requirements, product specifications, and quality standards. Key activities in this domain include the selection of appropriate packaging materials, designing labels with accurate and legible information, conducting rigorous packaging validations, and implementing quality assurance measures to mitigate packaging errors, defects, or discrepancies. Effective control over packaging and labeling is indispensable for maintaining product safety, integrity, and regulatory compliance, thereby safeguarding the product’s quality throughout the supply chain.
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