Autoclaves In Pharmaceutical Industry

In the pharmaceutical industry, the vertical high pressure steam sterilizer autoclave is an important piece of equipment to ensure production safety and product quality; it can sterilize the following items:

• Pharmaceutical industry laboratory applications: glassware, laboratory equipment, culture media, reagents, experimental samples, etc., to ensure that the experiments are pollution-free, to improve the accuracy of experiments

• A variety of sealed heat-resistant glass bottles or oral liquid filling infusion of high-temperature sterilization and rapid cooling operations, with water cooling and counter-pressure function, gentle cooling, to prevent the liquid from boiling and bursting bottles and bags.

• Working clothes: to ensure that employees wear sterile working clothes, to avoid contamination of the product.

• Experimental waste disposal: effectively kill microorganisms in the sample to ensure sterility and prevent pollution of the environment.

• Pharmaceutical package sterilization such as glass vials, medical bags, trays, cups, containers, ampoules and syringes sterilization, micro-sterilizer unique package program can meet the U.S. Pharmacopoeia USP660, the European Union Pharmacopoeia EP3.2.1 and the Chinese Pharmacopoeia on the demand for sterilization of pharmaceutical packages.

• Pharmaceutical and general cosmetics field: autoclave sterilization is widely used in cosmetics sterilization. High-pressure sterilization can kill bacteria, yeast, molds and other microorganisms, to ensure that the health and quality of cosmetics.

The application of autoclave sterilizers in pharmaceutical enterprises effectively protects the quality and safety of drugs and provides strong support for the development of pharmaceutical enterprises. As one of the professional pharmaceutical autoclave manufacturers, Zealway Autoclave can meet the stringent requirements of pharmaceutical enterprises for IQ/OQ/PQ validation and five-level management authority, as well as FDA 21 CFR Part 11 and electronic signature and other traceability requirements.