by Dr. Yashashwini Reddy | Oct 8, 2024
Tare Weight, Net Weight, and Gross Weight in the Pharmaceutical Industry: A Comprehensive Guide In the pharmaceutical industry, understanding tare weight, net weight, and gross weight is essential for maintaining product quality, ensuring regulatory compliance, and...
by Dr. Yashashwini Reddy | Sep 19, 2024
Japan’s new drug approval process is managed by the Pharmaceuticals and Medical Devices Agency (PMDA), which works under the Ministry of Health, Labour, and Welfare (MHLW). Here’s an overview of how a drug gets approved in Japan: 1. Preclinical Testing...
by Dr. Yashashwini Reddy | Sep 9, 2024
GMP vs. cGMP in Pharma: What’s the Difference? In the pharmaceutical world, making safe and high-quality medicines is essential. That’s where GMP (Good Manufacturing Practices) and cGMP (Current Good Manufacturing Practices) come in. While they sound similar, they...
by Dr. Yashashwini Reddy | Aug 13, 2024
“Understanding Master Copy, Control Copy, and Obsolete Copy in the Pharmaceutical Industry” In the Pharmaceutical industry document issue is very important and every document is traceable and accountable in the form of master copy, control copy, and...
by Dr. Yashashwini Reddy | Jul 11, 2024
Water is a major requirement for the pharmaceutical industry. We cannot imagine life without water and even in pharmaceutical manufacturing water is one of the most important requirements and based on the regulatory requirements the standards for water are...
