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Das Verfahren stellt sicher, dass Dampf jede Oberfläche mit der erforderlichen Temperatur und Einwirkdauer erreicht, um eine mikrobielle Abtötung zu gewährleisten.",[233],{"id":234,"title":235,"href":236,"type":48,"size":42,"arrow":237,"blockId":13,"fullWidth":12,"quizId":13,"icon":13,"lucideIcon":13},13960,"Mehr über SIP-Validierungsanforderungen erfahren","\u002Fsteam-in-place","right",{"__component":51,"id":239,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15847,{"__component":27,"id":241,"title":242,"content":243,"blockId":13,"ulStyle":31,"video":13,"auto play":32,"imageLeftTextRight":32,"preTitle":244,"preTitleColor":245,"ctaInfoText":13,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":32,"hideOnMobile":13,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":246,"media":13,"employee":13},14468,"Die Herausforderung der SIP-Validierung","### Validierung blockiert die Produktion\nDie SIP-Validierung erfordert, dass kritische Anlagen aus dem Produktionsbetrieb genommen werden – was zu Verzögerungen, Betriebsunterbrechungen und Umsatzeinbußen führt.\n\n### Komplexe Systeme sind komplex zu validieren\nDer Nachweis, dass Dampf jeden Punkt in Rohrleitungssystemen mit Transferleitungen, Verteilern und Toträumen erreicht, ist aufwendig und erfordert Fachkenntnisse.\n\n### Mehrere Anbieter verursachen Koordinationsverzögerungen\nDie herkömmliche SIP-Validierung erfordert die Koordination von Anlagen, Kalibrierung und Beratern. Jede Übergabe birgt das Potenzial für Fehler und Verzögerungen.","Das Problem","Capri Sun Dark",[],{"__component":51,"id":248,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15848,{"__component":27,"id":250,"title":251,"content":252,"blockId":13,"ulStyle":13,"video":13,"auto play":12,"imageLeftTextRight":12,"preTitle":253,"preTitleColor":254,"ctaInfoText":13,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":12,"hideOnMobile":12,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":255,"media":13,"employee":13},14472,"Die Steam-in-Place-Validierungslösung","Eupry bietet GMP-konforme SIP-Validierungsdienstleistungen für Hersteller aus der Pharma- und Biotechnologiebranche. Wir übernehmen die Kartierung, biologische Prüfung sowie die vollständige IQ\u002FOQ\u002FPQ für Ihre Anlagen.","Die Lösung","Mint Green Dark",[256],{"id":257,"title":46,"href":47,"type":48,"size":42,"arrow":43,"blockId":13,"fullWidth":12,"quizId":13,"icon":13,"lucideIcon":13},13961,{"__component":259,"id":260,"title":13,"lead":261,"iconStyle":13,"withBackground":12,"blockId":13,"ulStyle":13,"preTitle":13,"preTitleColor":254,"hideOnMobile":13,"layout":13,"iconItem":262},"blocks.icon-grid",2813,"",[263,269,274],{"id":264,"title":265,"lead":266,"icon":267,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":268,"lucideIcon":13,"showBackground":13},14510,"Vollständiger Validierungsservice","Eupry übernimmt die gesamte Validierung von IQ bis PQ. Wir platzieren Sensoren, koordinieren die Prüfungen, führen F0-Berechnungen durch und liefern vollständige Berichte.","CheckmarkCircle","Mint Green",{"id":270,"title":271,"lead":272,"icon":273,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":268,"lucideIcon":13,"showBackground":13},14511,"Validierung in der Hälfte der Zeit","Unsere Mapping-Kits und cloudbasierte Software ermöglichen es uns, die Validierung in der Hälfte der Zeit herkömmlicher Validierungsansätze abzuschließen.","Wifi",{"id":275,"title":276,"lead":277,"icon":278,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":268,"lucideIcon":13,"showBackground":13},14512,"Keine regulatorischen Lücken","Bewährte Protokolle und auf GMP spezialisierte Validierungsingenieure stellen sicher, dass Ihre Validierungen beim ersten Mal korrekt durchgeführt werden – jedes Mal.","DocumentPlus",{"__component":51,"id":280,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15849,{"__component":27,"id":282,"title":283,"content":284,"blockId":13,"ulStyle":13,"video":13,"auto play":12,"imageLeftTextRight":32,"preTitle":285,"preTitleColor":33,"ctaInfoText":13,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":32,"hideOnMobile":12,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":286,"media":13,"employee":13},14469,"Vollständige IQ\u002FOQ\u002FPQ-Gerätevalidierung","### Installationsqualifizierung (IQ)\nÜberprüfung der korrekten Installation gemäß Herstellerspezifikationen, Bestätigung der Versorgungsanforderungen (Dampfqualität, Druck, Durchfluss), Prüfung der Sicherheitssysteme und Dokumentation aller Messinstrumente mit nach ISO 17025 kalibrierter Ausrüstung.\n\n### Betriebsqualifizierung (OQ)\nValidierung des leeren Systems mit Dampfqualitätsprüfung (Trockenheit, nicht kondensierbare Gase, Überhitzung), Mehrpunkt-Mapping, Druckprüfung und Herausforderung des Steuerungssystems unter Normal- und Grenzbedingungen.\n\n### Leistungsqualifizierung (PQ)\nValidierung des beladenen Systems einschließlich Worst-Case-Tests, Wärmedurchdringungsstudien, biologischer Indikatoren und F0-Verifizierung (≥ 12 Minuten an allen Messpunkten).","So funktioniert es",[],{"__component":288,"id":289,"title":13,"content":13,"video":13,"blockId":13,"ulStyle":13,"preTitle":13,"preTitleColor":13,"titleLevel":34,"imageUrl":13,"subTitle":13,"videoAutoplay":32,"hideOnMobile":12,"ctaInfoText":13,"hideLastUpdated":13,"buttons":290,"media":13,"employee":13},"blocks.media-and-text",3915,[],{"__component":51,"id":292,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15850,{"__component":294,"id":295,"title":39,"content":296,"hubspotFormId":297,"blockId":298,"hubspotMeetingUrl":13,"titleLevel":34,"imageUrl":13,"hideOnMobile":13,"image":13},"blocks.contact-form",999,"Benötigen Sie weitere Informationen oder ein maßgeschneidertes Angebot? Füllen Sie das Formular aus, und wir werden uns so schnell wie möglich bei Ihnen melden.","f489cbd9-ab3d-4c0c-b7ae-a77950402417","contact",{"__component":51,"id":300,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15851,{"__component":259,"id":302,"title":303,"lead":13,"iconStyle":13,"withBackground":13,"blockId":13,"ulStyle":13,"preTitle":13,"preTitleColor":33,"hideOnMobile":13,"layout":13,"iconItem":304},2814,"Warum Eupry für die SIP-Validierung wählen?",[305,310,315,320],{"id":306,"title":307,"lead":308,"icon":267,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":309,"lucideIcon":13,"showBackground":13},14513,"Validierungsexpertise","Unsere Validierungsingenieure haben Hunderte von Qualifizierungen in pharmazeutischen Unternehmen durchgeführt und verstehen die regulatorischen Anforderungen der FDA-, EMA- und MHRA-Inspektoren.","Brain Freeze",{"id":311,"title":312,"lead":313,"icon":314,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":309,"lucideIcon":13,"showBackground":13},14514,"Vollständige Compliance","Jede Validierung umfasst eine ISO 17025-Kalibrierung mit NIST-Rückverfolgbarkeit, ISO 17665- und EN 285-konforme Protokolle, eine 21 CFR Part 11-fähige digitale Plattform sowie einen GMP-Anhang 15-konformen Qualifizierungsansatz.\n","CloudCheck",{"id":316,"title":317,"lead":318,"icon":319,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":309,"lucideIcon":13,"showBackground":13},14515,"Digitale Protokolle","Unser digitales Validierungssystem erfasst jeden Messwert mit Zeitstempel und Zuordnung, Kalibrierzertifikate sind eingebettet, und Sie können mit 3 Klicks vollständige Auditberichte mit lückenlosen Audit-Trails generieren.","Document1",{"id":321,"title":322,"lead":323,"icon":324,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":309,"lucideIcon":13,"showBackground":13},14516,"Eine Lösung für alle","Bei Eupry übernehmen wir die Validierung für jede temperaturgeführte Einheit oder Anlage im GMP- und GDP-Bereich – von Bioreaktoren und Tanks bis hin zu Autoklaven, Lagerhäusern und Kühlräumen. Ein Partner, alle Ihre Compliance-Anforderungen.","ArrowRight",{"__component":51,"id":326,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15852,{"__component":27,"id":328,"title":329,"content":330,"blockId":13,"ulStyle":31,"video":13,"auto play":12,"imageLeftTextRight":12,"preTitle":13,"preTitleColor":13,"ctaInfoText":331,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":32,"hideOnMobile":12,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":332,"media":13,"employee":13},14473,"Was wir validieren","- **Bioreaktoren und Fermenter**: Einwegsysteme und Edelstahlsysteme vom Labormaßstab bis zur Produktionsskala, mit Temperaturmapping, Dampfdurchdringungsverifizierung und Transferleitungsvalidierung.\n- **Tanks und Behälter**: Lager-, Puffer-, Misch- und Vorlagetanks für die Sterilproduktion, mit Überprüfung der Dampfabdeckung aller inneren Oberflächen und der ausreichenden Drainage.\n- **Transferleitungen und Verteiler**: Rohrleitungssysteme zur Verbindung von Prozessanlagen, mit Identifikation von Kaltpunkten, Verifizierung der Sterilisation von Totstrecken und Validierung von Dampffallen.\n- **CIP\u002FSIP-Systeme**: Integrierte Reinigungs- und Sterilisationssysteme, mit Validierung vollständiger Zyklen von CIP bis SIP hinsichtlich Reinigungs- und Sterilisationseffektivität.\n\nSowie alle weiteren kontrollierten Anlagen und Einrichtungen, die Sie im GMP-Umfeld benötigen.","Erhalten Sie spezifische Informationen zu Zeitplan und Preisen für Ihre Anlagen.",[333],{"id":334,"title":335,"href":40,"type":41,"size":42,"arrow":43,"blockId":13,"fullWidth":32,"quizId":13,"icon":13,"lucideIcon":13},13962,"Mit einem Validierungsspezialisten sprechen",{"__component":51,"id":337,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15853,{"__component":27,"id":339,"title":340,"content":341,"blockId":13,"ulStyle":13,"video":13,"auto play":12,"imageLeftTextRight":32,"preTitle":13,"preTitleColor":13,"ctaInfoText":13,"titleLevel":34,"imageUrl":13,"subTitle":342,"verticalCenteredText":32,"hideOnMobile":12,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":343,"media":13,"employee":13},14474,"Psst... Wir validieren auch Autoklaven","Benötigen Sie eine Autoklav-Validierung für Ihr Labor oder Ihre Produktionssterilisatoren? Wir bieten dieselben umfassenden IQ\u002FOQ\u002FPQ-Dienstleistungen für Dampfautoklaven – von Tischgeräten bis hin zu großen Produktionssterilisatoren.","(und jede andere GMP-Einheit oder -Anlage)",[344],{"id":345,"title":346,"href":347,"type":348,"size":42,"arrow":237,"blockId":13,"fullWidth":32,"quizId":13,"icon":13,"lucideIcon":13},13963,"So funktioniert der Autoklav-Validierungsservice","\u002Fsolutions\u002Fautoclave-validation\u002F","hot-pink",{"__component":51,"id":350,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15854,{"__component":352,"id":353,"title":46,"lead":354,"hubspotFormId":355,"blockId":356,"hubspotMeetingUrl":13,"titleLevel":34,"preTitle":13,"preTitleColor":13,"imageUrl":13,"hideOnMobile":13,"media":13},"blocks.download-form",3406,"Erhalten Sie einen einfachen Überblick über alle Produkte von Eupry – von der Validierung über die Kalibrierung bis hin zur automatisierten Überwachung von Temperatur, Luftfeuchtigkeit, CO2 und mehr.","76bf4d75-d529-402d-85d6-200a1bf95457","catalog",{"__component":51,"id":358,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15855,{"__component":27,"id":360,"title":361,"content":362,"blockId":13,"ulStyle":31,"video":13,"auto play":12,"imageLeftTextRight":32,"preTitle":13,"preTitleColor":13,"ctaInfoText":363,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":32,"hideOnMobile":13,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":364,"media":13,"employee":13},14475,"Ein Anbieter, alles was Sie für die thermische Compliance benötigen","Validierung, Überwachung und Kalibrierung in einer Lösung vereinen.\n\n- Bis zu 25 % niedrigere TCO\n- Eine einzige Datenquelle für alle Daten\n- Audit-Berichte mit 3 Klicks\n","Erhalten Sie sofortigen Zugang zu Informationen über die Funktionsweise der Lösungen und die technischen Spezifikationen.",[365],{"id":366,"title":367,"href":47,"type":48,"size":42,"arrow":43,"blockId":13,"fullWidth":12,"quizId":13,"icon":13,"lucideIcon":13},13964,"Jetzt einen Produktkatalog herunterladen",{"__component":51,"id":369,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},15856,{"__component":371,"id":372,"title":373,"content":13,"blockId":13,"preTitle":374,"preTitleColor":33,"includeInGoogleSchema":32,"hideOnMobile":13,"questions":375},"blocks.faq",2242,"FAQ zu Eupry's SIP-Validierungsdienstleistungen","Häufig gestellte Fragen",[376,380,384,388,392,396],{"id":377,"question":378,"answer":379},15113,"Welche Arten von Anlagen kann Eupry für SIP validieren?","Eupry validiert alle pharmazeutischen Dampfsterilisationssysteme: Bioreaktoren, Fermenter, Tanks, Behälter, Transferleitungen, Verteiler sowie CIP\u002FSIP-Systeme. Größen vom Labormaßstab (10 L) bis zum Produktionsvolumen (mehrere m³). Darüber hinaus alle weiteren temperaturgesteuerten Einheiten, Anlagen oder Einrichtungen, die für die GMP-konforme thermische Compliance erforderlich sind.",{"id":381,"question":382,"answer":383},15114,"Kann Eupry mehrere Anlagenkonfigurationen validieren?","Ja. Wir ermitteln die ungünstigsten Konfigurationen durch eine Risikobewertung und validieren repräsentative Aufbauten. Jede einzigartige Konfiguration erfordert eine separate Temperaturkartierung sowie Tests mit biologischen Indikatoren und einer dokumentierten Begründung.",{"id":385,"question":386,"answer":387},15115,"Was passiert, wenn wir einen SIP-Validierungstest nicht bestehen?","Fehler werden als Abweichungen mit Ursachenanalyse dokumentiert. Bei Eupry arbeiten wir gemeinsam mit Ihnen daran, das Problem zu beheben, und führen anschließend die betroffene Qualifizierungsphase erneut durch. Die Kosten für die Wiederholungsprüfung hängen vom Umfang des Fehlers ab.",{"id":389,"question":390,"answer":391},15116,"Wie lange dauert eine SIP-Validierung?","Der Zeitrahmen hängt von der Systemkomplexität und der Anzahl der Konfigurationen ab. Typische Zeitrahmen:\n- Einzelner Bioreaktor: 1–2 Wochen von der Mobilisierung bis zum Abschlussbericht\n- Mehrere Behälter oder komplexe Rohrleitungen: 3–4 Wochen\n- Standortübergreifende Validierungsprogramme: Individueller Zeitplan wird im Rahmen der Projektdefinition festgelegt\n\nWir stellen spezifische Zeitpläne und Projektterminpläne während der ersten Beratung bereit.",{"id":393,"question":394,"answer":395},15117,"Kann Eupry auch andere Geräte und Anlagen validieren?","Ja. Die Validierungsdienstleistungen von Eupry decken alle temperaturkontrollierten Einheiten und Einrichtungen in der Pharma-, Biotech- und Healthcare-Logistik ab – von Bioreaktoren und Autoklaven bis hin zu Lagerhäusern, Kühlräumen und Inkubatoren.\n\n[Laden Sie einen Produktkatalog herunter, um mehr über die Validierungsdienstleistungen von Eupry zu erfahren.](#catalog)",{"id":397,"question":398,"answer":399},15118,"Was kostet eine SIP-Validierung?","Die Preisgestaltung hängt von der Gerätegröße, der Komplexität, der Anzahl der validierten Zyklen und den Konfigurationsvarianten ab. Kontaktieren Sie uns für ein detailliertes Angebot basierend auf Ihren spezifischen Anforderungen. 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The process verifies that steam reaches every surface at the required temperature and duration to achieve microbial kill.",[537],{"id":538,"title":539,"href":236,"type":48,"size":42,"arrow":237,"blockId":13,"fullWidth":12,"quizId":13,"icon":13,"lucideIcon":13},12229,"Learn more about SIP validation requirements",{"id":541,"name":542,"alternativeText":543,"caption":13,"width":544,"height":545,"formats":546,"hash":554,"ext":75,"mime":78,"size":555,"url":556,"previewUrl":13,"provider":89,"provider_metadata":557,"createdAt":558,"updatedAt":559,"documentId":560,"publishedAt":561,"focalPoint":13},1861,"QUestion - wide - no bg.png","3D isometric question mark icon in dark navy and white with light purple shading on white background",1361,759,{"thumbnail":547},{"ext":75,"url":548,"hash":549,"mime":78,"name":550,"path":13,"size":551,"width":465,"height":466,"sizeInBytes":552,"provider_metadata":553},"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770128358\u002Fthumbnail_Q_Uestion_wide_no_bg_8dd024a260.png","thumbnail_Q_Uestion_wide_no_bg_8dd024a260","thumbnail_QUestion - wide - no bg.png",7.47,7471,{"public_id":549,"resource_type":85},"Q_Uestion_wide_no_bg_8dd024a260",31.78,"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770128358\u002FQ_Uestion_wide_no_bg_8dd024a260.png",{"public_id":554,"resource_type":85},"2026-02-03T14:19:19.479Z","2026-03-26T10:51:29.005Z","f07hfne5r8xtp96tv39r7076","2026-02-03T14:19:19.480Z",{"__component":51,"id":563,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},12766,{"__component":27,"id":565,"title":566,"content":567,"blockId":13,"ulStyle":31,"video":13,"auto play":32,"imageLeftTextRight":32,"preTitle":568,"preTitleColor":245,"ctaInfoText":13,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":32,"hideOnMobile":13,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":569,"media":570,"employee":13},12226,"The SIP validation challenge","### Validation blocks production\nSIP validation requires taking critical equipment out of production – meaning delays, disruptions, and lost revenue.\n\n### Complex systems are complex to validate\nProving steam reaches every location in piping systems with transfer lines, manifolds, and dead legs is complex and requires expertise.\n\n### Multiple vendors create coordination delays\nTraditional SIP validation involves coordinating equipment, calibration, and consultants. Each handoff creates potential for errors and delays.","The problem",[],{"id":571,"name":572,"alternativeText":573,"caption":13,"width":574,"height":575,"formats":576,"hash":585,"ext":75,"mime":78,"size":586,"url":587,"previewUrl":13,"provider":89,"provider_metadata":588,"createdAt":589,"updatedAt":590,"documentId":591,"publishedAt":592,"focalPoint":13},1453,"Alarm.png","Isometric illustration of a red alarm siren with lightning bolt symbols indicating an active alert",1200,794,{"thumbnail":577},{"ext":75,"url":578,"hash":579,"mime":78,"name":580,"path":13,"size":581,"width":582,"height":82,"sizeInBytes":583,"provider_metadata":584},"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1760017434\u002Fthumbnail_Alarm_b10a2f10b1.png","thumbnail_Alarm_b10a2f10b1","thumbnail_Alarm.png",7.01,236,7010,{"public_id":579,"resource_type":85},"Alarm_b10a2f10b1",53.66,"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1760017435\u002FAlarm_b10a2f10b1.png",{"public_id":585,"resource_type":85},"2025-10-09T13:43:55.961Z","2026-03-26T11:16:46.771Z","trsbtxf5lwln5jp4haf9j351","2025-10-09T13:43:55.962Z",{"__component":51,"id":594,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},12767,{"__component":27,"id":596,"title":597,"content":598,"blockId":13,"ulStyle":13,"video":13,"auto play":12,"imageLeftTextRight":12,"preTitle":599,"preTitleColor":254,"ctaInfoText":13,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":12,"hideOnMobile":12,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":600,"media":603,"employee":13},12336,"The steam-in-place validation solution","Eupry provides GMP-compliant SIP validation services for pharmaceutical and biotech manufacturers. We handle mapping, biological testing, and complete IQ\u002FOQ\u002FPQ for your equipment.","The solution",[601],{"id":602,"title":452,"href":47,"type":48,"size":42,"arrow":43,"blockId":13,"fullWidth":12,"quizId":13,"icon":13,"lucideIcon":13},12230,{"id":604,"name":605,"alternativeText":606,"caption":13,"width":607,"height":608,"formats":609,"hash":617,"ext":75,"mime":78,"size":618,"url":619,"previewUrl":13,"provider":89,"provider_metadata":620,"createdAt":621,"updatedAt":622,"documentId":623,"publishedAt":621,"focalPoint":13},1864,"Platform mobile + desktop - software - SIP VERSION.png","Eupry temperature monitoring dashboard on tablet showing data logger graphs, alarms, and logbook entries for Position 01",1386,1081,{"thumbnail":610},{"ext":75,"url":611,"hash":612,"mime":78,"name":613,"path":13,"size":614,"width":142,"height":82,"sizeInBytes":615,"provider_metadata":616},"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770145498\u002Fthumbnail_Platform_mobile_desktop_software_SIP_VERSION_b3bf801978.png","thumbnail_Platform_mobile_desktop_software_SIP_VERSION_b3bf801978","thumbnail_Platform mobile + desktop - software - SIP VERSION.png",15.17,15173,{"public_id":612,"resource_type":85},"Platform_mobile_desktop_software_SIP_VERSION_b3bf801978",147.28,"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770145500\u002FPlatform_mobile_desktop_software_SIP_VERSION_b3bf801978.png",{"public_id":617,"resource_type":85},"2026-02-03T19:05:13.818Z","2026-03-26T11:02:38.916Z","tshoq2nollfwwrbns4ratimv",{"__component":259,"id":625,"title":13,"lead":261,"iconStyle":13,"withBackground":12,"blockId":13,"ulStyle":13,"preTitle":13,"preTitleColor":254,"hideOnMobile":13,"layout":13,"iconItem":626},2379,[627,631,635],{"id":628,"title":629,"lead":630,"icon":267,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":268,"lucideIcon":13,"showBackground":13},12552,"Complete validation service","Eupry handles the full validation from IQ through PQ. We place sensors, manage testing, perform F0 calculations, and deliver complete reports.",{"id":632,"title":633,"lead":634,"icon":273,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":268,"lucideIcon":13,"showBackground":13},12553,"Validation in half the time","Our mapping kits and cloud-based software let us complete validation in half the time of traditional validation approaches.",{"id":636,"title":637,"lead":638,"icon":278,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":268,"lucideIcon":13,"showBackground":13},12554,"Zero regulatory gaps","Proven protocols and GMP-specialized validation engineers ensures your validations are done right the first time - every time.",{"__component":51,"id":640,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},12768,{"__component":27,"id":448,"title":642,"content":643,"blockId":13,"ulStyle":13,"video":13,"auto play":12,"imageLeftTextRight":32,"preTitle":644,"preTitleColor":33,"ctaInfoText":13,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":32,"hideOnMobile":12,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":645,"media":646,"employee":13},"Complete IQ\u002FOQ\u002FPQ equipment validation","### Installation qualification (IQ)\nVerify correct installation per manufacturer specifications, confirm utility requirements (steam quality, pressure, flow), test safety systems, and document all instrumentation with ISO 17025 calibrated equipment.\n\n### Operational qualification (OQ)\nEmpty system validation with steam quality verification (dryness, non-condensable gases, superheat), multi-point mapping, pressure testing, and control system challenge under normal and edge conditions.\n\n### Performance qualification (PQ)\nLoaded system validation including worst-case testing, heat penetration studies, biological indicators, and F0 verification (≥ 12 minutes at all locations).","How it works",[],{"id":647,"name":648,"alternativeText":649,"caption":13,"width":650,"height":651,"formats":652,"hash":661,"ext":75,"mime":78,"size":662,"url":663,"previewUrl":13,"provider":89,"provider_metadata":664,"createdAt":665,"updatedAt":666,"documentId":667,"publishedAt":668,"focalPoint":13},1857,"IQ, OQ, PQ2.png","Light blue gradient background with bold text reading IQ, OQ & PQ in white and teal tones",1178,833,{"thumbnail":653},{"ext":75,"url":654,"hash":655,"mime":78,"name":656,"path":13,"size":657,"width":658,"height":82,"sizeInBytes":659,"provider_metadata":660},"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770124318\u002Fthumbnail_IQ_OQ_PQ_2_d8fc27faeb.png","thumbnail_IQ_OQ_PQ_2_d8fc27faeb","thumbnail_IQ, OQ, PQ2.png",28.85,221,28846,{"public_id":655,"resource_type":85},"IQ_OQ_PQ_2_d8fc27faeb",229.71,"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770124317\u002FIQ_OQ_PQ_2_d8fc27faeb.png",{"public_id":661,"resource_type":85},"2026-02-03T13:11:59.117Z","2026-03-26T10:49:04.512Z","yrujlp3fgvn3zrspcfep1olg","2026-02-03T13:11:59.118Z",{"__component":288,"id":670,"title":13,"content":13,"video":13,"blockId":13,"ulStyle":13,"preTitle":13,"preTitleColor":13,"titleLevel":34,"imageUrl":13,"subTitle":13,"videoAutoplay":32,"hideOnMobile":12,"ctaInfoText":13,"hideLastUpdated":13,"buttons":671,"media":672,"employee":13},3253,[],{"id":673,"name":674,"alternativeText":675,"caption":13,"width":676,"height":677,"formats":678,"hash":687,"ext":75,"mime":78,"size":688,"url":689,"previewUrl":13,"provider":89,"provider_metadata":690,"createdAt":691,"updatedAt":692,"documentId":693,"publishedAt":691,"focalPoint":13},1819,"Eupry Stats banner - NEW - Jan 2026.png","Eupry stats banner showing 50+ countries, 6000+ monitored locations, 1000+ companies, and leading EU calibration lab",1886,306,{"thumbnail":679},{"ext":75,"url":680,"hash":681,"mime":78,"name":682,"path":13,"size":683,"width":465,"height":684,"sizeInBytes":685,"provider_metadata":686},"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1769422006\u002Fthumbnail_Eupry_Stats_banner_NEW_Jan_2026_156a5f6d0e.png","thumbnail_Eupry_Stats_banner_NEW_Jan_2026_156a5f6d0e","thumbnail_Eupry Stats banner - NEW - Jan 2026.png",19.69,40,19687,{"public_id":681,"resource_type":85},"Eupry_Stats_banner_NEW_Jan_2026_156a5f6d0e",344.56,"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1769422006\u002FEupry_Stats_banner_NEW_Jan_2026_156a5f6d0e.png",{"public_id":687,"resource_type":85},"2026-01-26T10:06:47.318Z","2026-03-26T11:10:04.814Z","syzxq63wtohowfycpcp0sr0q",{"__component":51,"id":695,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},12769,{"__component":294,"id":697,"title":449,"content":698,"hubspotFormId":297,"blockId":298,"hubspotMeetingUrl":13,"titleLevel":34,"imageUrl":13,"hideOnMobile":13,"image":699},811,"Need more information or a tailored quote? Fill out the form, and we will be in touch as soon as possible.",{"id":700,"name":701,"alternativeText":702,"caption":13,"width":703,"height":704,"formats":705,"hash":714,"ext":75,"mime":78,"size":715,"url":716,"previewUrl":13,"provider":89,"provider_metadata":717,"createdAt":718,"updatedAt":719,"documentId":720,"publishedAt":718,"focalPoint":13},1573,"People for contact form.png","Three Eupry team members in circular profile photos: a young woman, an older man, and a younger man",508,385,{"thumbnail":706},{"ext":75,"url":707,"hash":708,"mime":78,"name":709,"path":13,"size":710,"width":711,"height":82,"sizeInBytes":712,"provider_metadata":713},"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1778230569\u002Fthumbnail_People_for_contact_form_9539e227c2.png","thumbnail_People_for_contact_form_9539e227c2","thumbnail_People for contact form.png",46.94,206,46940,{"public_id":708,"resource_type":85},"People_for_contact_form_9539e227c2",180.17,"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1778230569\u002FPeople_for_contact_form_9539e227c2.png",{"public_id":714,"resource_type":85},"2025-11-28T08:24:27.705Z","2026-05-08T08:56:09.725Z","cqp4ka41xxouuvrz8zun78vs",{"__component":51,"id":722,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},12770,{"__component":259,"id":724,"title":725,"lead":13,"iconStyle":13,"withBackground":13,"blockId":13,"ulStyle":13,"preTitle":13,"preTitleColor":33,"hideOnMobile":13,"layout":13,"iconItem":726},2380,"Why choose Eupry for SIP validation?",[727,731,735,739],{"id":728,"title":729,"lead":730,"icon":267,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":309,"lucideIcon":13,"showBackground":13},12555,"Validation expertise","Our validation engineers have conducted hundreds of qualifications across pharmaceutical companies and understand the regulatory expectations from FDA, EMA, and MHRA inspectors.",{"id":732,"title":733,"lead":734,"icon":314,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":309,"lucideIcon":13,"showBackground":13},12556,"Complete compliance","Every validation comes with ISO 17025 calibration with NIST traceability, ISO 17665 and EN 285 compliant protocols, 21 CFR Part 11-ready digital platform, and GMP Annex 15 aligned qualification approach.\n",{"id":736,"title":737,"lead":738,"icon":319,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":309,"lucideIcon":13,"showBackground":13},12557,"Digital protocols","Our digital validation system captures every reading with timestamps and attribution, calibration certificates are embed, and you can generate complete audit reports in 3 clicks with full audit trails.",{"id":740,"title":741,"lead":742,"icon":324,"linkTitle":13,"linkHref":13,"ulStyle":13,"backgroundColor":309,"lucideIcon":13,"showBackground":13},12558,"One solution for all","At Eupry, we handle validation for any temperature-controlled unit or facility in GMP and GDP – from bioreactors and tanks to autoclaves, warehouses, and cold rooms. One partner, all your compliance needs.",{"__component":51,"id":744,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},12771,{"__component":27,"id":746,"title":747,"content":748,"blockId":13,"ulStyle":31,"video":13,"auto play":12,"imageLeftTextRight":12,"preTitle":13,"preTitleColor":13,"ctaInfoText":749,"titleLevel":34,"imageUrl":13,"subTitle":13,"verticalCenteredText":32,"hideOnMobile":12,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":750,"media":754,"employee":13},12337,"What we validate","- **Bioreactors and fermenters**: Single-use and stainless steel systems from benchtop to production scale, with temperature mapping, steam penetration verification, and transfer line validation.\n- **Tanks and vessels**: Storage, buffer, mixing, and holding tanks for sterile production, verifying steam coverage to all internal surfaces and drainage adequacy.\n- **Transfer lines and manifolds**: Piping systems connecting process equipment, with cold spot identification, dead leg sterilization verification, and steam trap validation.\n- **CIP\u002FSIP systems**: Integrated cleaning and sterilization systems, validating complete cycles from CIP through SIP for cleaning and sterilization effectiveness.\n\nAnd any other controlled equipment and facility you need in GMP.","Get specific timeline and pricing information for your equipment.",[751],{"id":752,"title":753,"href":40,"type":41,"size":42,"arrow":43,"blockId":13,"fullWidth":32,"quizId":13,"icon":13,"lucideIcon":13},12231,"Talk to a validation specialist ",{"id":755,"name":756,"alternativeText":757,"caption":13,"width":458,"height":758,"formats":759,"hash":768,"ext":75,"mime":78,"size":769,"url":770,"previewUrl":13,"provider":89,"provider_metadata":771,"createdAt":772,"updatedAt":773,"documentId":774,"publishedAt":772,"focalPoint":13},1860,"SIP validation.png","Stainless steel bioreactor vessel with piping in a pharmaceutical cleanroom, technician in white protective gear operating controls",600,{"thumbnail":760},{"ext":75,"url":761,"hash":762,"mime":78,"name":763,"path":13,"size":764,"width":765,"height":82,"sizeInBytes":766,"provider_metadata":767},"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770127261\u002Fthumbnail_SIP_validation_719ec778c9.png","thumbnail_SIP_validation_719ec778c9","thumbnail_SIP validation.png",81.5,191,81500,{"public_id":762,"resource_type":85},"SIP_validation_719ec778c9",781,"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770127262\u002FSIP_validation_719ec778c9.png",{"public_id":768,"resource_type":85},"2026-02-03T13:56:48.601Z","2026-03-26T10:49:55.174Z","gnl2suyydasz06njrfm6m0h7",{"__component":51,"id":776,"divider":32,"blockId":13,"hideOnMobile":13,"spacing":13},12772,{"__component":27,"id":778,"title":779,"content":780,"blockId":13,"ulStyle":13,"video":13,"auto play":12,"imageLeftTextRight":32,"preTitle":13,"preTitleColor":13,"ctaInfoText":13,"titleLevel":34,"imageUrl":13,"subTitle":781,"verticalCenteredText":32,"hideOnMobile":12,"hideTopDecoration":13,"hideLastUpdated":13,"buttons":782,"media":786,"employee":13},12338,"Psst... We also validate autoclaves","Need autoclave validation for your laboratory or manufacturing sterilizers? We provide the same complete IQ\u002FOQ\u002FPQ services for steam autoclaves – from benchtop units to large production sterilizers.","(and any other GMP unit or facility)",[783],{"id":784,"title":785,"href":347,"type":348,"size":42,"arrow":237,"blockId":13,"fullWidth":32,"quizId":13,"icon":13,"lucideIcon":13},12232,"See how the autoclave validation service works",{"id":787,"name":788,"alternativeText":789,"caption":13,"width":790,"height":791,"formats":792,"hash":801,"ext":75,"mime":78,"size":802,"url":803,"previewUrl":13,"provider":89,"provider_metadata":804,"createdAt":805,"updatedAt":806,"documentId":807,"publishedAt":808,"focalPoint":13},1865,"Autoclave validation - no logos.png","Pharma technician in cleanroom gear loading vials into autoclave with sterilization monitoring dashboard overlay",1508,975,{"thumbnail":793},{"ext":75,"url":794,"hash":795,"mime":78,"name":796,"path":13,"size":797,"width":798,"height":82,"sizeInBytes":799,"provider_metadata":800},"https:\u002F\u002Fres.cloudinary.com\u002Feupry\u002Fimage\u002Fupload\u002Fv1770278572\u002Fthumbnail_Autoclave_validation_no_logos_294be635b7.png","thumbnail_Autoclave_validation_no_logos_294be635b7","thumbnail_Autoclave validation - 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