Journal of Research and Development
Open Access
ISSN: 2311-3278
ISSN: 2311-3278
Pakistan
Extended Abstract
Euro analytica 2020: Pharmaceutical Impurity Analysis of Raw Materials and Final Product by using analytical techniques - Muhammad Jehangir - Novamed Pharmaceuticals.
Author(s): Muhammad Jehangir
Isolation and identification of unknown components and impurities” The evaluation of pharmaceutical raw materials and finished products for impurities and degradation products is an essential part of the drug development and manufacturing testing process. Additionally, toxicological information must be obtained on any drug-related impurity that is present at a concentration of greater than 0.1% of that of the active pharmaceutical ingredient (API). In pharmaceutical QC and manufacturing, impurity analysis has traditionally been performed by HPLC with UV, PDA, or MS detection. As it is essential to detect and measure all of the impurities in the sample, it is necessary to have a high resolution separation process. This usually .. View More»