医薬品分析化学: オープンアクセス
オープンアクセス

概要

医薬品不純物プロファイリングにおける包括的な品質保証のための多変量解析の統合

ラヴィ・シャー

In the field of pharmaceuticals, ensuring product safety and efficacy is most important. Impurity profiling, the process of identifying and quantifying impurities in pharmaceutical products, stands as a basis of quality assurance protocols. This article delves into the significance of impurity profiling, its methodologies, regulatory aspects, and its pivotal role in safeguarding public health.