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This e-book leads you step by step through the 4 key processes in microbiological monitoring.Additionally you will get a detailed look at monitoring and testing in 3 critical areas: surfaces, personnel and air.
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Excerpt from the GMP Compliance Adviser This just-released report provides you with the essential in-depth knowledge you need to correctly monitor the hygienic status of your sterile drug sites and evaluate your cleaning and disinfecting measures. Step by step, you'll go through the 4 key monitoring processes
And you'll get a detailed look at monitoring and testing 3 critical areas: surfaces, personnel and air. The report also covers monitoring and testing utilities, cleansing agents and disinfectants. Specifically, you'll learn how to set alert and action limits and the measures to take if those limits are exceeded. And you'll get in-depth coverage of:
It's all here in the most thorough report available: everything you need to know to successfully monitor, investigate and mitigate contamination risks at drug manufacturing plants and stay in compliance with FDA and EU regulations.
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This file is in PDF format!Filesize: 1,92 MB
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A Guide to Control Microbial Risks in Sterile and Aseptic Drug Manufacturing
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