by Dr. Yashashwini Reddy | Apr 11, 2025
Isn’t it amazing to be alive right now? We have answers to almost any question at our fingertips, thanks to the tiny device we carry in our hands. However, even with all these incredible resources, things don’t always go as planned, and we still face...
by Dr. Yashashwini Reddy | Nov 11, 2024
Fishbone Diagram in the Pharmaceutical Industry: A Simple Guide Creating a Fishbone Diagram, also known as an Ishikawa or Cause-and-Effect Diagram, is a great way to visually break down and understand the causes of a problem in pharmaceutical processes. This tool is...
by Dr. Yashashwini Reddy | Nov 1, 2024
Importance of Critical Process Parameters (CPPs) in Pharmaceutical Manufacturing Critical Process Parameters (CPPs) are key to ensuring product quality in the pharmaceutical industry. These parameters—such as temperature, pH, mixing speed, and pressure—are closely...
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...
by Dr. Yashashwini Reddy | May 15, 2024
In-process checks during compression by QA The IPQA person is responsible for performing the in-process checks at a predetermined frequency along with the production personnel to ensure quality products are consistently produced. As you know pharmaceutical products...
