{"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\/?p=2047","title":{"rendered":"IQ IN ETO STERILIZATION PROCESS"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">Het Iq in eto-sterilisatieproces wordt uitgevoerd om aan te tonen dat de sterilisatieapparatuur en eventuele bijbehorende artikelen zijn geleverd en geïnstalleerd in overeenstemming met hun specificatie. Voordat IQ wordt uitgevoerd, voert de fabrikant van de apparatuur FAT en SAT uit om ervoor te zorgen dat de apparatuur normaal is afgeleverd.<\/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\">Tijdens IQ moeten de volgende gebeurtenissen verder worden geïdentificeerd en onderbouwd.<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">a. Apparatuur die bij het sterilisatieproces wordt gebruikt, inclusief eventuele aanvullende items, moet voldoen aan de ontwerpspecificaties. De bijbehorende documenten omvatten functionele ontwerpspecificaties, specificaties van gebruikersvereisten, ontwerptekeningen, enz. (Schema van de apparatuur, diagram van de energievoorziening, elektrisch schema, schematisch diagram van het systeem, enz.)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">b.Controleer of alle componenten (inclusief besturingssoftware) naar behoren functioneren; Belangrijke meetinstrumenten moeten worden gekalibreerd; Belangrijke componentinformatie moet worden vastgelegd;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">c.Zorg ervoor dat de installatie- en gebruiksomgeving veilig is en voldoet aan de plaatselijke regelgeving. Voldoe aan de veiligheids- en gezondheidseisen van het personeel.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">d.Documenten voor veiligheidsproductie en werkprocedures ontwikkelen, inclusief documenten voor onderhoud en afhandeling van uitzonderingen; het geven van operatortrainingen; operators kunnen pas aan de slag nadat ze gekwalificeerd zijn.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">e. IQ kan een eenmalige oefening zijn voor de specifieke apparatuur die wordt gebruikt voor een sterilisatieproces.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">F. Er moet ook extra IQ worden uitgevoerd in het geval van significante componentveranderingen of functionele veranderingen<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-if-you-want-to-know-more-about-iq-in-eto-sterilization-process\">ALS U MEER WILT WETEN OVER IQ IN HET ETO-STERILISATIEPROCES<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">Telefoon:<a href=\"https:\/\/wa.me\/8619975258603\">+8619975258603<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">E-mail:<a href=\"mailto:hayley@hzbocon.com\">hayley@hzbocon.com<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Lokale locatie: kamer 1202, Caitong Zhongxin, Xiasha District, Hangzhou City, provincie Zhejiang, China<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Website:<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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Technical Team","author_link":"https:\/\/zjbocon.com\/?author=234312599"},"uagb_comment_info":17,"uagb_excerpt":"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.)","jetpack_likes_enabled":true,"jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/pgZDV6-x1","jetpack-related-posts":[{"id":2013,"url":"https:\/\/zjbocon.com\/?p=2013","url_meta":{"origin":2047,"position":0},"title":"Purpose for eto sterilization validation","author":"Bocon Technical Team","date":"2024-10-28","format":false,"excerpt":"1.Purpose\u00a0for validation eto sterilization 1.1.the obtain of eto sterilization validation evidence that the equipment used for ETO sterilization has been provided and installed in accordance with its specification and can stably operate within predetermined limits and consistently performs in accordance with predetermined criteria and thereby yields product meeting its specification.\u2026","rel":"","context":"In &quot;ETO STERILIZER&quot;","block_context":{"text":"ETO STERILIZER","link":"https:\/\/zjbocon.com\/?cat=133124"},"img":{"alt_text":"eto sterilization validation","src":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2024\/10\/Qualification_Services-2.webp?resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2024\/10\/Qualification_Services-2.webp?resize=350%2C200 1x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2024\/10\/Qualification_Services-2.webp?resize=525%2C300 1.5x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2024\/10\/Qualification_Services-2.webp?resize=700%2C400 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