Currently browsing "QMS"
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Best Practices for Aligning Pharmaceutical QMS with FDA’s Quality Metrics Initiative
Introduction Regulatory compliance and operational excellence have long been “talking the same talk in the pharmaceutical sector.” One of its essential constituencies, the FDA Quality Metrics Initiative, indicates a vital turning point toward generic manufacturing and distribution process quality standards. Compliance is not the end of the road. Manufacturers are also taking a data-driven, proactive […]
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Ensuring Compliance with FDA, EMA, and Global Regulatory Bodies through QMS
Successful pharmaceutical and medical device industry operations in a globalized world necessitate meeting stringent regulatory requirements. Such standards are not merely legal obligations but the cornerstones for safety, efficacy, and output quality. Regulatory bodies like the FDA, EMA, and other national and international bodies create regimes to secure and safeguard public health from dangerous products. […]
