by Dr. Yashashwini Reddy | Jul 8, 2024
Change management in the pharmaceutical industry: Companies always strive for innovation and continual improvement, and sometimes based on the output of process performance, quality monitoring, and CAPA drive changes in the process or systems. A proper change control...
by Dr. Yashashwini Reddy | May 30, 2024
SOP ON ROLES AND RESPONSIBILITIES OF QA DEPARTMENT 1.0 Objective: To outline the roles and responsibilities of the quality assurance department 2.0 Scope: This SOP shall be applicable to Personnel working in quality assurance and activities of QA department. 3.0...
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...
