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...
by Dr. Yashashwini Reddy | May 14, 2024
In this article we are going to learn routine activity performed by IPQA Personnel in Tablet compression area Introduction: In-Process Quality Assurance Person is responsible for line clearance activities and in this article, we are going to learn what activities he...
