PQ is a leading global provider of silicates, silicas and derivative products that are friendlier and contribute to a cleaner, safer world. Qualification refers to activities undertaken to demonstrate that utility and equipment are suitable for their intended use and performing properly. Qualification Definition: It is the action of providing and documenting that equipment or ancillary systems are properly installed, work correctly, and accurately leading to the expected results. Qualification is a part of validation but individual qualification alone does not constitute process validation. All pharmaceutical companies are required to abide by stringent regulations to ensure their products are safe and effective. Regulatory authorities specifically emphasize on qualification processes in pharma manufacturing facilities. The process of qualification aims to ensure that all aspects of the equipment being used meet regulatory and operational requirements. Moreover, it verifies that the equipment and instrument used are fit for their intended purpose. DQ, IQ, OQ, and PQ, the four ... How to Conduct Performance Qualification in Pharma What is Performance Qualification (PQ) in Pharmaceutical Manufacturing? Performance Qualification (PQ) is a critical phase in the process of validating pharmaceutical equipment and systems. It involves testing the equipment and systems under actual production conditions to verify that they consistently perform according to the defined specifications and produce the desired product quality. PQ ensures that the equipment performs reliably ...
