Evaluating Impurities in Drugs (Part II of III) - Pharmaceutical Technology

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Evaluating Impurities in Drugs (Part II of III)

Pharmaceutical Technology Europe
Volume 24, Issue 3

By Kashyap R. Wadekar, Mitali Bhalme, S. Srinivasa Rao, K. Vigneshwar Reddy, L. Sampath Kumar, E. Balasubrahmanyam

The public and the pharmaceutical industry are placing greater attention on impurities in drug as evidenced by the attention given to pharmaceutical impurities in books, journal articles, and national and international guidelines. The health implications of impurities can be significant because of their potential teratogenic, mutagenic, or carcinogenic effects. Controlling and monitoring impurities in APIs and finished drug products, therefore, is a crucial issue in drug development and manufacturing.

This article was also published in our US sister publication Pharmaceutical Technology and can be read here.

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