{"id":9914,"date":"2025-06-23T19:13:36","date_gmt":"2025-06-23T17:13:36","guid":{"rendered":"https:\/\/dandiag.dk\/?p=9914"},"modified":"2026-04-08T16:51:27","modified_gmt":"2026-04-08T14:51:27","slug":"vaegtkalibrering-i-pharma-saadan-sikrer-du-compliance-og-praecision","status":"publish","type":"post","link":"https:\/\/demo.hviiddigital.dk\/dandiag.dk\/viden\/artikler\/vaegtkalibrering-i-pharma-saadan-sikrer-du-compliance-og-praecision\/","title":{"rendered":"V\u00e6gtkalibrering i pharma: S\u00e5dan sikrer du compliance og pr\u00e6cision"},"content":{"rendered":"\n<p><strong>Hvorfor pr\u00e6cise v\u00e6gte er kritiske i pharma<\/strong><\/p>\n\n\n\n<p>I pharmaindustrien er der ikke plads til upr\u00e6cise m\u00e5linger. Selv den mindste afvigelse i v\u00e6gt kan have store konsekvenser for b\u00e5de kvalitet, sikkerhed og lovgivningsm\u00e6ssig compliance. Derfor er v\u00e6gtkalibrering ikke bare en teknisk n\u00f8dvendighed \u2013 det er en forretningskritisk proces.<\/p>\n\n\n\n<p>Hos Dandiag m\u00f8der vi ofte laboratorier, der \u00f8nsker st\u00f8rre sikkerhed i deres m\u00e5linger og mindre risiko ved inspektioner. Svaret starter med \u00e9n ting: en kalibreret v\u00e6gt, der er dokumenteret i henhold til de rigtige standarder.<\/p>\n\n\n\n<p><strong>Regulatoriske krav og ISO-standarder<\/strong><\/p>\n\n\n\n<p>I pharma er det ikke nok at vide, at en v\u00e6gt plejer at veje korrekt. Du skal kunne dokumentere, at den vejer korrekt \u2013 og det p\u00e5 det rigtige tidspunkt.<\/p>\n\n\n\n<p>V\u00e6gtkalibrering i pharma skal typisk leve op til f\u00f8lgende krav:<\/p>\n\n\n\n<p><strong>\u00b7 ISO 17025-akkreditering<\/strong>: Sikrer at kalibrering foretages af et kompetent og uafh\u00e6ngigt laboratorium.<br><strong>\u00b7 GMP og GDP<\/strong>: L\u00e6gger v\u00e6gt p\u00e5 sporbarhed, dokumentation og kvalitet i m\u00e5leudstyr.<br>\u00b7 <strong>EURAMET CG-18<\/strong>: Guideline for fasts\u00e6ttelse af kalibreringsintervaller og v\u00e6gtklassifikation.<\/p>\n\n\n\n<p>Er du i tvivl, om dine v\u00e6gte lever op til kravene? S\u00e5 er det v\u00e6rd at gennemg\u00e5 b\u00e5de din dokumentation og dine aftaler med kalibreringsleverand\u00f8ren.<\/p>\n\n\n\n<p><strong>Hvad sker der, hvis v\u00e6gten er un\u00f8jagtig?<\/strong><\/p>\n\n\n\n<p>I pharma er pr\u00e6cision ikke et sp\u00f8rgsm\u00e5l om komfort \u2013 det handler om patientsikkerhed. Et forkert vejefundament kan f\u00f8re til:<\/p>\n\n\n\n<p>\u00b7 Fejldosering i formulering<br>\u00b7 Ugyldige testresultater<br>\u00b7 Oml\u00f8b og tabte batches<br>\u00b7 Kritiske findings ved audits og inspektioner<\/p>\n\n\n\n<p>En v\u00e6gt, der bare afviger med 0,2 mg, kan i sidste ende koste tusindvis af kroner \u2013 eller dit GMP-rygte.<\/p>\n\n\n\n<p><strong>Hvad er god praksis for v\u00e6gtkalibrering i pharma?<\/strong><\/p>\n\n\n\n<p>Hos Dandiag anbefaler vi f\u00f8lgende praksis:<\/p>\n\n\n\n<p>\u00b7 Akkrediteret kalibrering \u00e9n gang \u00e5rligt<br>\u00b7 \u201cAs found\u201d og \u201cas left\u201d-m\u00e5linger, s\u00e5 du kan dokumentere evt. afvigelser f\u00f8r justering<br>\u00b7 Kalibrering ved brugspunkter \u2013 ikke kun ved max kapacitet<br>\u00b7 Dokumentation og certifikater i overensstemmelse med ISO 17025 og sporbarhedskrav<\/p>\n\n\n\n<p><strong>Dandiags rolle i pharma-industrien<\/strong><\/p>\n\n\n\n<p>Vi kalibrerer v\u00e6gte for nogle af Danmarks mest kr\u00e6vende pharma- og life science-virksomheder. Med ISO 17025-akkreditering, over 25 \u00e5rs erfaring og et team, der kender b\u00e5de v\u00e6gte og regulering i dybden, tilbyder vi r\u00e5dgivning og service, du kan regne med \u2013 b\u00e5de f\u00f8r, under og efter kalibreringen.<\/p>\n\n\n\n<p><\/p>\n\n\n\n<p><strong>Er dine v\u00e6gte kalibreret korrekt \u2013 og dokumenteret til inspektion?<\/strong><\/p>\n\n\n\n<p> Kontakt os i dag og f\u00e5 en uforpligtende gennemgang af dine v\u00e6gte og jeres compliance-behov.<\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Hvorfor pr\u00e6cise v\u00e6gte er kritiske i pharma I pharmaindustrien er der ikke plads til upr\u00e6cise m\u00e5linger. Selv den mindste afvigelse i v\u00e6gt kan have store konsekvenser for b\u00e5de kvalitet, sikkerhed og lovgivningsm\u00e6ssig compliance. Derfor er v\u00e6gtkalibrering ikke bare en teknisk n\u00f8dvendighed \u2013 det er en forretningskritisk proces. Hos Dandiag m\u00f8der vi ofte laboratorier, der \u00f8nsker&#8230;<\/p>\n","protected":false},"author":60,"featured_media":334,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[1],"tags":[2535,2375,2346],"class_list":["post-9914","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized","tag-compliance","tag-kalibrering","tag-vaegte"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>V\u00e6gtkalibrering i pharma: S\u00e5dan sikrer du compliance og pr\u00e6cision - Dandiag (Demo)<\/title>\n<meta name=\"description\" content=\"Akkrediteret v\u00e6gtkalibrering er afg\u00f8rende i pharma. 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