BAS EN ISO 11737-1:2019
Sterilizacija medicinskih sredstava - Mikrobiološke metode - Dio 1: Određivanje broja mikroorganizama na proizvodima
Opće informacije
Status: Važeći
Broj strana: 51
Jezik: Engleski
Izdanje: 2.
Metoda usvajanja: Proglašavanje
Nadnevak objave: 11.06.2019
Tehnički komitet:
Direktiva:
2017/745, Uredba (EU) o medicinskim sredstvima;
2017/746, Uredba (EU) o medicinskim sredstvim u in vitro dijagnostici
2017/746, Uredba (EU) o medicinskim sredstvim u in vitro dijagnostici
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Apstrakt
ISO 11737-1:2018 specifies requirements and provides guidance on the enumeration and microbial characterization of the population of viable microorganisms on or in a health care product, component, raw material or package.
NOTE 1 The nature and extent of microbial characterization is dependent on the intended use of bioburden data.
NOTE 2 See Annex A for guidance on Clauses 1 to 9.
ISO 11737-1:2018 does not apply to the enumeration or identification of viral, prion or protozoan contaminants. This includes the removal and detection of the causative agents of spongiform encephalopathies, such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease.
NOTE 3 Guidance on inactivating viruses and prions can be found in ISO 22442‑3, ICH Q5A(R1) and ISO 13022.
ISO 11737-1:2018 does not apply to the microbiological monitoring of the environment in which health care products are manufactured.
Životni ciklus
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Izvorni dokument i stepen usklađenosti
- EN ISO 11737-1:2018, identičan
- ISO 11737-1:2018, identičan