Study of Development and Quantification Process for Toxic Metal Impurity Assessment in Pharmaceuticals

Abstract

This study presents a crucial investigation into the development and quantification of processes aimed at assessing toxic metal impurities in pharmaceutical products. The presence of toxic metals in pharmaceuticals can pose severe health risks to patients, making their accurate detection and quantification of paramount importance.The research begins by addressing the development aspect, emphasizing the creation of robust methodologies and protocols for the identification and measurement of toxic metal impurities. This step is critical in ensuring the reliability and consistency of results, which is essential for pharmaceutical safety.the study delves into the quantification process, which involves determining the concentration levels of