All Content

Nonconformities and CAPA: how to ensure the quality and safety of drugs in the pharmaceutical industry

In the highly regulated pharmaceutical industry, every process, however controlled it may be, is subject to deviations, occurrences or unusual production situations that can impact product quality. These deviations pose a serious threat to the efficacy, safety and quality of drugs and should be addressed as nonconformities. In this article, we will discuss the importance … Continue reading “Nonconformities and CAPA: how to ensure the quality and safety of drugs in the pharmaceutical industry”

Read more