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<p>ISO/TS 19930:2017 provides guidance on identifying the aspects to be considered as part of a risk-based approach to selecting a sterility assurance level (SAL) for terminally sterilized, single-use health care product that is unable to withstand processing to achieve maximally a SAL of 10−6.</p>
<p>In addition, this document provides</p>
<p>a) background information on the assurance of sterility and sterility assurance level, and</p>
<p>b) guidance on strategies that can allow the achievement of a maximal SAL of 10−6.</p>
<p>ISO/TS 19930:2017 describes the elements of a quality management system which are applied to enable the appropriate selection of a SAL for terminally sterilized, single-use health care product that is unable to withstand processing to achieve maximally a SAL of 10−6.</p>
<p>NOTE It is not a requirement of the International Standards for development, validation and routine control of a sterilization process to have a full quality management system. Attention is drawn to the standard for quality management systems (see ISO 13485) that controls all stages of the lifecycle of health care product.</p>
<p>ISO/TS 19930:2017 is applicable to sterilization processes in which microorganisms are inactivated by physical and/or chemical means.</p>
<p>ISO/TS 19930:2017 does not apply</p>
<p>- to selecting a maximal SAL greater than 10−6 for health care product that is able to withstand processing to achieve maximally a SAL of 10−6;</p>
<p>- in cases where a maximal SAL of 10−6 is required and an alternative SAL is not allowed;</p>
<p>- in cases where a maximal SAL of greater than 10−6 (e.g. 10−3) has been accepted by regulatory authorities within their jurisdiction for health care product for defined use;</p>
<p>- to the sterilization of used or reprocessed health care product;</p>
<p>- to sterilization of health care product by filtration.</p>
<p>ISO/TS 19930:2017 does not describe detailed procedures for assessing microbial inactivation.</p>
<p>ISO/TS 19930:2017 does not specify requirements for the development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease. Specific recommendations have been produced in particular countries for the processing of materials potentially contaminated with these agents.</p>
<p>NOTE See also ISO 22442‑1, ISO 22442‑2 and ISO 22442‑3.</p>
<p>ISO/TS 19930:2017 does not supersede or modify published International Standards for particular sterilization processes. ISO/TS 19930:2017 neither recommends a SAL for a given health care product nor identifies a maximal SAL for a health care product to be labelled "sterile".</p>
<p>NOTE These are matters for regulatory authorities and can vary from country to country.</p>
Reģistrācijas numurs (WIID)
66566
Darbības sfēra
<p>ISO/TS 19930:2017 provides guidance on identifying the aspects to be considered as part of a risk-based approach to selecting a sterility assurance level (SAL) for terminally sterilized, single-use health care product that is unable to withstand processing to achieve maximally a SAL of 10−6.</p>
<p>In addition, this document provides</p>
<p>a) background information on the assurance of sterility and sterility assurance level, and</p>
<p>b) guidance on strategies that can allow the achievement of a maximal SAL of 10−6.</p>
<p>ISO/TS 19930:2017 describes the elements of a quality management system which are applied to enable the appropriate selection of a SAL for terminally sterilized, single-use health care product that is unable to withstand processing to achieve maximally a SAL of 10−6.</p>
<p>NOTE It is not a requirement of the International Standards for development, validation and routine control of a sterilization process to have a full quality management system. Attention is drawn to the standard for quality management systems (see ISO 13485) that controls all stages of the lifecycle of health care product.</p>
<p>ISO/TS 19930:2017 is applicable to sterilization processes in which microorganisms are inactivated by physical and/or chemical means.</p>
<p>ISO/TS 19930:2017 does not apply</p>
<p>- to selecting a maximal SAL greater than 10−6 for health care product that is able to withstand processing to achieve maximally a SAL of 10−6;</p>
<p>- in cases where a maximal SAL of 10−6 is required and an alternative SAL is not allowed;</p>
<p>- in cases where a maximal SAL of greater than 10−6 (e.g. 10−3) has been accepted by regulatory authorities within their jurisdiction for health care product for defined use;</p>
<p>- to the sterilization of used or reprocessed health care product;</p>
<p>- to sterilization of health care product by filtration.</p>
<p>ISO/TS 19930:2017 does not describe detailed procedures for assessing microbial inactivation.</p>
<p>ISO/TS 19930:2017 does not specify requirements for the development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease. Specific recommendations have been produced in particular countries for the processing of materials potentially contaminated with these agents.</p>
<p>NOTE See also ISO 22442‑1, ISO 22442‑2 and ISO 22442‑3.</p>
<p>ISO/TS 19930:2017 does not supersede or modify published International Standards for particular sterilization processes. ISO/TS 19930:2017 neither recommends a SAL for a given health care product nor identifies a maximal SAL for a health care product to be labelled "sterile".</p>
<p>NOTE These are matters for regulatory authorities and can vary from country to country.</p>
