by Dr. Yashashwini Reddy | May 5, 2025
The quality of pharmaceutical products is crucial for ensuring their safety, efficacy, and reliability. When pharmaceuticals are substandard, they pose significant health risks, including treatment failures, adverse reactions, and even death. Various factors can...
by Dr. Yashashwini Reddy | May 3, 2025
Generic drugs manufacturing: opportunities and obstacles Introduction- Generic drugs are an essential part of the healthcare system, providing a more affordable alternative to brand-name medications. As patents for branded drugs expire, generic manufacturers can...
by Dr. Yashashwini Reddy | May 3, 2025
Tablet Manufacturing Process: An Overview The tablet manufacturing process is a complex and precise procedure that transforms raw materials into the final pharmaceutical or nutraceutical product. The process involves several key stages, each critical to ensuring the...
by Dr. Yashashwini Reddy | Apr 29, 2025
Quality issues in the pharmaceutical industry can arise from a variety of sources across the entire lifecycle of drug development, manufacturing, and distribution. Below is a detailed breakdown of the root causes: 1. Manufacturing Process Failures Inadequate Process...
by Dr. Yashashwini Reddy | Nov 28, 2024
Out of Specifications (OOS) in Pharmaceuticals Out of Specification (OOS) results occur when the test results of a pharmaceutical product fall outside the predefined acceptance criteria specified in regulatory guidelines or quality standards. These deviations are...
