by Naveen kumar | 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 Naveen kumar | 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 Naveen kumar | 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...
by Naveen kumar | May 3, 2024
Identifying the root cause of the problem is very important. In pharmaceuticals Root cause analysis is an invaluable tool to dig deep and identify the origin of the problem. To perform Root cause analysis, different techniques are used. that I’m going to mention...
