DIN EN ISO 13408-7:2015 Edition
$34.45
Aseptische Herstellung von Produkten für die Gesundheitsfürsorge – Teil 7: Alternative Verfahren für Medizinprodukte und Kombinationsprodukte
Published By | Publication Date | Number of Pages |
DIN | 2015-11 | 38 |
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Dieser Teil von ISO 13408 legt Anforderungen fest und stellt Leitlinien für alternative Ansätze zur Prozesssimulation für die Qualifikation aseptischer Prozesse von Medizinprodukten und Kombinations-Produkten auf, die nicht endsterilisiert werden können und wo der Ansatz der Prozesssimulation nach ISO 13408-1 nicht angewendet werden kann. Dieser Teil von ISO 13408 beschreibt, wie die Risikobewertung während der Entwicklung eines aseptischen Prozesses erstellt werden kann, um eine Studie zur Prozesssimulation für Medizinprodukte und Kombinations-Produkte für die Fälle zu entwickeln, bei denen ein direkten Ersatz von Medien für das Produkt während der aseptischen Verarbeitung nicht möglich ist oder wo der tatsächliche aseptische Prozess nicht simuliert werden kann.*Inhaltsverzeichnis
Published Code | DIN |
---|---|
Published By | Deutsches Institut für Normung |
Publication Date | 2015-11 |
Pages Count | 38 |
Language | Germany |
Descriptors | Anforderung, Aseptik, Begriffe, CE-Kennzeichnung, Definition, Gesundheitsdienst, keimarm, Medizin, medizinisches Instrument, Medizinprodukt, Medizintechnik, Qualitätssicherung, Reinigung, Sterilität |
File Size | 1.9 MB |
ICS Codes | 11.080.01 - Sterilization and disinfection in general |
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