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- W2319629555 abstract "The purpose of Quality Risk Management is to illustrate practical ways to analyze the risks to quality system, providing guidance along the way to achieving effective and efficient quality management and compliance. In the pharmaceutical manufacturing every product and every process associated with risks. To maintain product quality throughout the product life cycle, too much time and resources are allocated. Risk is described in -recent guidance as a combination of the probability of occurrence of harm and the severity of that harm. The Quality Risk Management (QRM) approach initiated by regulatory agencies with recognized management tools along with support of statistical tools in combination allows for a risk-based approach to quality management, thus ensuring that resources are deployed in a timely and expeditious manner to areas that need them most and proactive approach to compliance of good manufacturing practices (GMP)." @default.
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- W2319629555 date "2014-01-01" @default.
- W2319629555 modified "2023-10-03" @default.
- W2319629555 title "Implementation of Quality Risk Management (QRM) In Pharmaceutical Manufacturing Industry" @default.
- W2319629555 doi "https://doi.org/10.9790/3008-091495101" @default.
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