In the world of medical device manufacturing, quality and safety aren’t just goals, they’re requirements. That’s where IQ, OQ, and PQ come in. These aren’t just letters; they’re essential quality assurance protocols that ensure the equipment used to make medical devices is installed correctly (IQ), operating as it should (OQ), and performing consistently (PQ).
Validation is critical in regulated industries like medical device manufacturing, where producing safe and effective products is paramount. So, what exactly are IQ, OQ, and PQ? Why do they matter? And how are they put into practice? This article will break it down.