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Eurofins Medical Device Testingc/o Eurofins BioPharma Product Testing Munich GmbH
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- Über uns
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Unser Angebot
- Biokompatibilitätsprüfungen nach ISO 10993
- Chemische Charakterisierung
- Mechanische Prüfungen
- Mikrobiologie für Medizinprodukte
- Physikalisch-chemische Prüfungen
- Risikoanalyse und Toxikologische Bewertung
- in vitro Hemocompatibility testing
- Schulungen und Seminare
- Sonstige Dienstleistungen
- Reinigung, Montage, Verpackung und Sterilisation von Medizinprodukten
- Validierte Methoden
- Downloads
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News & Events
- Messen und Konferenzen
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Seminare, Webinare und Workshops
- LIVE WEBINAR: Blood is not just blood - Why a Predicate Sample is recommended in Hemocompatibility Testing
- SEMINAR: The Times They Are A-Changing – in vitro Testing in Biocompatibility
- LIVE WEBINAR: Biocompatibility testing of breathing gas pathway devices (ISO 18562 and ISO 10993)
- LIVE WEBINAR S(p)oiler Alarm – Reusable Medical Devices, how to proceed and what is new?
- LIVE WEBINAR MDR submission for your Medical Device
- Extractables und Leachables - Keeping Up to Speed!
- S(p)oiler Alarm – wiederaufbereitbare Medizinprodukte, was nun?
- MDR submission for your Medical Device - How to climb Mount Regulatory?
- Chemical Characterization: Current Status of Recent Changes and Some Interpretations
- Biological Safety Spotlight: Surface-contacting Medical Devices
- Biological Safety Spotlight: External Communicating Devices.
- Biological Safety Spotlight: Implant Devices.
- Biokompatibilität von Medizinprodukten - Neueste Änderungen in der ISO 10993er Reihe und Einfluss auf die Teststrategie
- Validation of Reprocessing for Reusable Medical Devices: Requirements, Possibilities and Limits
- ISO 10993-23 Update: Irritation Testing Strategies and Results Interpretation
- ISO 10993-12:2021: Going into details of sample preparation
- Biocompatibility of Raw Materials – What Data Should Your Supplier Provide?
- Testing of antimicrobial properties of medical devices
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