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MasterControl Audit Brochure
2013-08-28 05:16:20| drugdiscoveryonline Home Page
A quality audit is to a regulated company what a medical examination is to a patient. It is a necessary and repeating procedure for evaluating a quality system’s general “health” and for “diagnosing” problems in order to correct them. In the FDA and ISO environments, quality audits are required on an ongoing basis to help improve product quality and safety — and to ensure compliance.
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Category:Biotechnology and Pharmaceuticals