In the pharmaceutical and clinical industries, even a slight mistake can lead to serious problems. Therefore, in the pharmaceutical, medical device and clinical industries, they should be strictly regulated. In order to ensure the safety and quality of equipment in production and operation, operational qualification and performance qualification are proposed and strictly stipulated. Performance Qualification VS Operational Qualification-sourced: csolsinc What is operational qualification and performance qualification? Why they are important? ...

If you are in the process of getting GMP standard, you may know the performance qualification which also called as PQ in many place. It is the qualification which test the processing performance of your industry. You cannot ignore it if you want to make your manufacturing process reliable and efficient. How much you know about it? Why you need performance qualification? What industry can performance qualification be applied? What ...

There are many processes involved in the production and commissioning of equipment. Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) serve as two vital stages. The completion of acceptance at these two stage represents that the machine is qualified. How much do you know about these two types of acceptance testings? Why are these two acceptance testing means so important? Are you curious about the similarities and differences between ...

Drying is an integral step in the preparation of different ingredients, especially solid dosage forms. Vacuum drying has significance in drying raw material by lowering the temperature of solvents, leading to energy conservation. Isn't that sustainable? How vacuum drying is carried out? The lab vacuum dryer is a dynamic device that quickly and uniformly dries different ingredients- from pharmaceuticals to foodstuff. What are its pros? What are its types? Several ...

Are you trying to install equipment? Are you trying to minimize hazardous risks during installation? Installation is a must before successfully operating the equipment. Effective installation guarantees the smooth performance of any device. One must follow manufacturer specifications and recommendations to ensure error-free installation. How to verify that the installation conforms with standards? Installation qualification is an indispensable procedure that ensures the instrument and systems' safety, quality, functioning, and reliability. ...

Have you ever heard of DQ, IQ, OQ, or PQ? In FDA-Regulated industries, every piece of equipment and system is hooked to proper regulations. This means each step and protocol is jotted down in specified protocols. Why is it required to have verified documentation? What happens if your equipment is missing functional specifications? In this article, we have talked about from basic to advanced literature about DQ, IQ, OQ, PQ ...

Wait a second! Are you in search of a guide that gives you whole information about chlorine tablet press machine? Here you got it! This 'Chlorine Tablet Press Machine: The Complete Buying Guide In 2025' will cover every aspect of the main theme. Starting from its introduction, it will tell you its benefits, applications, elements, operation method, maintenance and important factors that you should consider before buying this machine. Let ...

Are you interested in knowing about protein powder making machine? If yes, you are at the right place and at the right time. We have something new and comprehensive for you related to your interest. This guide is best for you whether you are a beginner or owning a big firm. Protein powder making is one of the growing industries worldwide and its utilization is immense in the current age. ...