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DSF/EN ISO 11737-1/PRA1

Sterilization of health care products – Microbiological methods – Part 1: Determination of a population of microorganisms on products – Amendment 1 (ISO 11737-1:2018/DAM 1:2019)

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Organization: DS
Status: inactive
Page Count: 6
ICS Code (Medical microbiology): 07.100.10
ICS Code (Sterilization and disinfection in general): 11.080.01
scope:

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.

Document History

June 21, 2021
Sterilization of health care products – Microbiological methods – Part 1: Determination of a population of microorganisms on products – Amendment 1 (ISO 11737-1:2018/Amd 1:2021)
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,...
February 6, 2018
Sterilization of health care products – Microbiological methods – Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2018)
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,...
May 11, 2009
Sterilization of medical devices – Microbiological methods – Part 1: Determination of a population of microorganisms on products
This standard specifies requirements and provides guidance for the enumeration and and characterization of the population of viable microorganisms on or in a medical device, component, raw material...
March 31, 2006
Sterilization of medical devices – Microbiological methods – Part 1: Determination of a population of microorganisms on products
This standard specifies requirements and provides guidance for the enumeration and and characterization of the population of viable microorganisms on or in a medical device, component, raw material...
Sterilization of health care products – Microbiological methods – Part 1: Determination of a population of microorganisms on products (ISO/FDIS 11737-1:2017)
This part of ISO 11737 specifies requirements and provides guidance for the enumeration and microbial characterization of the population of viable microorganisms on or in a health care product,...
Sterilization of health care products – Microbiological methods – Part 1: Determination of a population of microorganisms on products – Amendment 1 (ISO 11737-1:2018/FDAM 1:2020)
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,...
DSF/EN ISO 11737-1/PRA1
Sterilization of health care products – Microbiological methods – Part 1: Determination of a population of microorganisms on products – Amendment 1 (ISO 11737-1:2018/DAM 1:2019)
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,...
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