Blog
Kapil D2023-08-03T05:18:17+00:00Welcome to SynThink Blog.
Here, we keep you posted about the latest updates and insights into pharmaceutical impurities. We understand that impurities in pharmaceuticals can significantly impact their safety and efficacy, and it is crucial to maintain stringent standards to ensure quality of the products. Our blog site provides the most accurate and up-to-date information on impurity standards, regulations, and guidelines in the pharmaceutical industry. We hope you find our blogs informative and valuable.
Difference between Process-Related and Degradation-Related Impurities
Dr. Wazurkar2023-12-19T06:52:48+00:00Difference between Process Impurities and Degradation Impurities
Understanding the distinctions between Process Impurities and Degradation Impurities is crucial in pharmaceutical development and quality assurance. These impurities,...Structure Elucidation of Unknown Impurity using LC-MS/MS
Dr. Wazurkar2023-12-18T08:17:50+00:00Structure Elucidation of Unknown Impurity using LC-MS/MS in Pharmaceuticals
I. Introduction
Impurity analysis in pharmaceuticals is a critical quality control measure. Impurities, arising during synthesis, storage, or...
Advancements in LC-MS Technology
Dr. Wazurkar2023-12-18T08:54:41+00:00
Advancements in LC-MS Technology: Transforming Pharmaceutical Analysis
Introduction
Liquid Chromatography-Mass Spectrometry (LC-MS or LC/MS or LCMS) is an indispensable technology in the realm of pharmaceutical analysis. It...The Nitrosamine puzzle: What We Learned in the Last Five Years
Dr. Wazurkar2023-08-29T10:48:44+00:00
