Aging facilities in pharmaceutical manufacturing are a topic of much concerned discussion in the industry and in world healthcare circles, especially where sterile and potent products are produced. Facility conditions and obsolete technologies pose risks to product quality and, therefore, supply of medicines to patients. Facility finishes, aging water systems, manual cleaning methods, and presence of gowned personnel in the aseptic environment performing open process manipulations all contribute to process risks and the potential exposure of potent products.
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