Automate Pharmaceutical Quality Control and Comply with 21 CFR Part 11

22 Jul 2020

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Pharmaceutical manufacturers are always looking for ways to automate processes to save money and speed production. However, they must perform these steps in a manner that complies with 21 CFR part 11, which can sometimes be difficult, especially when conducting water quality testing and environmental monitoring. Data integrity must also be considered, as data is what drives compliance. One of the areas in which many pharmaceutical companies encounter problems during audits is the 21 CFR part 11 .. continue reading data integrity issues due to employees not following SOPs in a manual process. Thus, Pharmaceutical manufacturers are looking for ways to automate processes to analyze purified water or water for injection (commonly known as WFI) and also environmental monitoring of non-viable particles in clean areas. Automating these processes will help the pharmaceutical manufacturer reduce errors, maintain compliance, and maintain data integrity.


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100 - 500
Based on previous editions

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Medical & Pharma


22 Jul 2020

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Salman Ali

Salman Ali

M.pharamcy at gurunanak university

Hyderabad, India

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