by Dr. Yashashwini Reddy | May 2, 2025
Equipment malfunction in pharmaceutical production can have wide-ranging and serious implications, affecting not only operational efficiency but also regulatory compliance, product quality, and patient safety. Here’s a detailed explanation of how such malfunctions can...
by Dr. Yashashwini Reddy | May 28, 2024
Departure from an approved procedure, instruction, or documented procedure is called deviation. A deviation should be properly documented and handled. A deviation can occur during the manufacturing, testing, storage, or distribution of pharmaceuticals. Deviations most...
