{"id":2047,"date":"2024-10-30T11:16:45","date_gmt":"2024-10-30T03:16:45","guid":{"rendered":"https:\/\/zjbocon.com\/?p=2047"},"modified":"2025-12-05T11:16:43","modified_gmt":"2025-12-05T03:16:43","slug":"iq-in-eto-sterilization-process","status":"publish","type":"post","link":"https:\/\/zjbocon.com\/iq-in-eto-sterilization-process\/","title":{"rendered":"IQ IN ETO STERILIZATION PROCESS"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">Eto 멸균 공정의 Iq는 멸균 장비 및 보조 품목이 해당 사양에 따라 공급 및 설치되었음을 입증하기 위해 수행됩니다. IQ를 수행하기 전에 장비 제조업체는 FAT 및 SAT를 수행하여 장비가 정상적으로 배송되었는지 확인합니다.<\/p>\n\n\n\n<div class=\"wp-block-uagb-image uagb-block-a3122174 wp-block-uagb-image--layout-default wp-block-uagb-image--effect-static wp-block-uagb-image--align-none\"><figure class=\"wp-block-uagb-image__figure\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/zjbocon.com\/wp-content\/uploads\/2025\/09\/Ethylene-Oxide-Sterilizer-Installation-Guide-1-1024x473.webp\" alt=\"\" class=\"uag-image-8475\" width=\"1024\" height=\"473\" title=\"Ethylene-Oxide-Sterilizer-Installation-Guide-1\" role=\"img\" \><\/figure><\/div>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-during-iq-the-following-events-need-to-be-further-identified-and-substantiated\">IQ 동안 다음 사건을 추가로 식별하고 입증해야 합니다.<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">a.부속 품목을 포함하여 멸균 과정에 사용되는 장비는 설계 사양을 준수해야 합니다. 해당 문서에는 기능 설계 사양, 사용자 요구 사항 사양, 설계 도면 등이 포함됩니다. (장비 개략도, 에너지 공급 다이어그램, 전기 개략도, 시스템 개략도 등)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">b.모든 구성요소(제어 소프트웨어 포함)가 제대로 작동하는지 확인합니다. 주요 측정 장비를 교정해야 합니다. 주요 구성요소 정보를 기록해야 합니다.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">c. 설치 및 사용 환경이 안전하고 현지 규정을 준수하는지 확인하십시오. 안전 및 직원 건강 요구 사항을 충족합니다.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">d. 유지보수 및 예외 처리 문서를 포함한 안전 생산 및 운영 절차 문서를 개발합니다. 운영자 교육을 실시합니다. 운영자는 자격을 갖춘 후에만 작업을 시작할 수 있습니다.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">이자형. IQ는 멸균 과정에 사용되는 특정 장비에 대한 일회성 연습일 수 있습니다.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">에프. 중요한 구성 요소 변경이나 기능 변경이 있는 경우에도 추가 IQ를 수행해야 합니다.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-if-you-want-to-know-more-about-iq-in-eto-sterilization-process\">ETO 멸균 과정의 IQ에 대해 더 알고 싶다면<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">핸드폰:<a href=\"https:\/\/wa.me\/8619975258603\">+8619975258603<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">이메일:<a href=\"mailto:hayley@hzbocon.com\">hayley@hzbocon.com<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">현지 사이트: 중국 절강성 항저우시 샤사구 차이통 중신 1202호<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">웹사이트:<a href=\"https:\/\/www.hzbocon.com\/\">hzbocon.com<\/a><a href=\"https:\/\/zjbocon.com\/\">zjbocon.com<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>a.Equipment to be used in the sterilization process, including any\u00a0ancillary 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.)<\/p>\n","protected":false},"author":234312599,"featured_media":8475,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_uag_custom_page_level_css":"","site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center 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Re-qualification Frequency \u2022\u00a0Minimum annual requirement\u2022 At least once per year, verification data, subsequent re-validation data, and routine processing data must be reviewed\u2022 The scope of re-qualification must be determined and documented\u2022 The review procedure shall be documented 2. 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Ethylene oxide cylinders should be stored separately in a dry, well-ventilated room, with strict prohibition of smoking and open flames. The lighting in the sterilization chamber should be explosion-proof, and any electrical appliances that may cause electric\u2026","rel":"","context":"In &quot;Company News&quot;","block_context":{"text":"Company News","link":"https:\/\/zjbocon.com\/category\/company-news\/"},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2024\/10\/Electrical-Scale.png?resize=350%2C200","width":350,"height":200},"classes":[]},{"id":8776,"url":"https:\/\/zjbocon.com\/how-to-test-eto-gas-sterilization-test-materials\/","url_meta":{"origin":2047,"position":5},"title":"How to Test ETO Gas Sterilization Test Materials","author":"Bocon Technical Team","date":"2025-11-25","format":false,"excerpt":"When it comes to ETO gas sterilization, testing is an essential part of ensuring the effectiveness and safety of the sterilization process. 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