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Class zero air: achieving sustainability goals while ensuring compliant product quality

机译:Zero Zero Air:在确保符合产品质量的同时实现可持续发展目标

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摘要

Traditionally, compressed air has had several shortcomings that impact drug manufacturing and handling, such as high maintenance costs, a significant risk of contamination and the presence of moisture. Compressed air quality in a pharmaceutical manufacturing process is directly related to end-product quality. Previously, pharmaceutical companies were afforded the luxury of simply paying the additional price to ensure this quality. Nowadays, they need to balance the rising costs and energy emissions of the plant while, at the same time, maintaining product quality and process efficiency. This means that they're now challenging existing norms and looking for innovative solutions to their quality compressed air needs.
机译:传统上,压缩空气有几种影响药物制造和处理的缺点,例如高维护成本,污染的显着风险和水分的存在。 药物制造过程中的压缩空气质量与最终产品质量直接相关。 此前,制药公司奢侈品只需支付额外的价格,以确保这种质量。 如今,他们需要平衡植物的上升成本和能源排放,同时保持产品质量和工艺效率。 这意味着他们现在正在挑战现有的规范,并寻找他们的质量压缩空气需求的创新解决方案。

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