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Titlebook: Good Manufacturing Practice in Transfusion Medicine; Proceedings of the E C. Th. Smit Sibinga,P. C. Das,H. J. Heiniger Conference proceedin

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樓主: 淺吟低唱
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發(fā)表于 2025-3-30 09:09:37 | 只看該作者
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Good Manufacturing Practice and Blood Derivatives: Requirements and Mechanisms for Product Licensinglness throughout the world. The achievement (or non-achievement) of this overall quality objective entirely depends on Good Manufacturing Practices (GMP). Moreover, these GMPs themselves form an integral component of the concept of Quality Assurance (QA), within which they are combined with Good Lab
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Standards and External Quality Audit Systemstions of regulatory or peer review groups responsible for setting those standards, and the methods for determining whether all facilities comply with the applicable standards. Most workers in all countries would agree, however, that “external audits”, (or “inspections” in the blood banker’s usual ja
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