PQ is the stage of validation that uses Ethylene oxide sterilization chamber to demonstrate that the Ethylene oxide sterilization equipment consistently operates in accordance with predetermined acceptance criteria and the process yields a product that is sterile and meets the specified requirements.
In OQ, the performance of the relevant auxiliary system should be determined and the software system should be tested by simulating the fault conditions.
a.Equipment to be used in the sterilization process, including any ancillary items, shall comply with its design specifications.The corresponding documents include functional design specifications, user requirements specifications, design drawings, etc. (Equipment schematic diagram, energy supply diagram, electrical schematic diagram, system schematic diagram, etc.)
IQ IN ETO STERILIZATION PROCESS Read more
Ethylene oxide sterilizer operate at low temperatures, making them ideal for sterilizing heat-sensitive medical devices and instruments. This characteristic allows for the preservation of the integrity and functionality of complex medical devices that might be damaged by heat.
The advantage of Ethylene oxide sterilizer Read more
Protection mechanism and explanation OF ETO Sterilizer System 2. By default, the system will perform the leak detection test before
1.Purpose for validation eto sterilization 1.1.the obtain of eto sterilization validation evidence that the equipment used for ETO sterilization has been
ethylene oxide in sterilization Introduction ETO is a colorless gas that is flammable and explosive. The four essential parameters (operational
The Detail EtO Sterilization Cycle A typical EtO sterilization cycle comprises three main stages: Preconditioning This stage prepares the chamber
環氧乙烷（EtO 或 EO）滅菌是一種無色氣體，廣泛應用於不同行業，包括材料、個人護理用品的生產以及治療設備、化妝品和香料的環氧乙烷滅菌。 EtO 是對恢復器具進行消毒的重要策略，在避免接受手術方法和其他恢復治療的患者受到污染方面發揮著至關重要的作用。