by Dr. Yashashwini Reddy | Sep 29, 2024
“Essential Regulatory Affairs Interview Questions for Freshers in Pharma: Tips & Answers” 1. What is an Abbreviated New Drug Application (ANDA)? Answer: An Abbreviated New Drug Application (ANDA) is a regulatory submission to gain approval for a...
by Dr. Yashashwini Reddy | Sep 23, 2024
In the pharmaceutical industry, clean rooms are more than just sterile environments; they are critical spaces designed to keep our products safe from contamination. One of the unsung heroes in these clean rooms is the air lock. Think of it as a buffer zone that helps...
by Dr. Yashashwini Reddy | Sep 20, 2024
In pharmaceutical manufacturing, blending plays a key role in ensuring that drugs are safe, effective, and of high quality. This process involves thoroughly mixing active pharmaceutical ingredients (APIs) with excipients (inactive ingredients) to ensure uniform...
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 10, 2024
Tablets vs. Capsules: What’s the Difference? If you’ve ever taken medication, chances are you’ve encountered both tablets and capsules. Though both are common forms of delivering medicine, they differ in several ways. Let’s break down the differences: 1....
