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Risikomanagement und Biologische Sicherheit von Medizinprodukten

Am Beispiel der biologischen Bewertung und unter Einbeziehung der DIN EN ISO 10993-1 und DIN EN ISO 14971
Edition 2022-01

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Qualitätsmanagement für Hersteller von Medizinprodukten

Praxisleitfaden zur DIN EN ISO 13485 und den neuen EU-Verordnungen
Edition 2019-04

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Sterilisation von Medizinprodukten

Indikatoren und Verpackungen für in der Endverpackung zu sterilisierende Medizinprodukte
Edition 2020-12

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