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Automated Aseptic Production Systems


Life Science | March 30, 2012

PDF | 2 pages | 734 KB

cover page for the ATS Automated Aseptic Brochure


Manufacturers are keenly aware of the serious implications and potential consequences that poor cGMP conditions and excursions from process sterility can have on aseptic production. Automated processes, particularly those in barriered or isolated environments represent the best way to manage contamination risk and provide the added benefit of increased productivity, minimal batch-to-batch variation, yield improvement and, in the case of clinical volumes, an easy route to scale up.


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