（清空日期可显示全部记录）
| 标准编号 | 标准名称 | 发布日期 | 实施日期 | 废止日期 | 替换信息 |
|---|---|---|---|---|---|
| ISO 15189:2003 | Medical laboratories -- Particular requirements for quality and competence | ||||
| ISO/TS 19218-1:2011 | Medical devices -- Hierarchical coding structure for adverse events -- Part 1: Event-type codes | ||||
| ISO/TS 19218:2005 | Medical devices -- Coding structure for adverse event type and cause | ||||
| ISO/TS 19218-2:2012 | Medical devices -- Hierarchical coding structure for adverse events -- Part 2: Evaluation codes | ||||
| ISO 22870:2016 | Point-of-care testing (POCT) -- Requirements for quality and competence | ||||
| ISO/IEC Guide 23:1982 | Methods of indicating conformity with standards for third-party certification systems | ||||
| ISO Guide 27:1983 | Guidelines for corrective action to be taken by a certification body in the event of misuse of its mark of conformity | ||||
| ISO/IEC Guide 28:1982 | General rules for a model third-party certification system for products | ||||
| ISO/IEC Guide 28:2004 | Conformity assessment -- Guidance on a third-party certification system for products | ||||
| ISO/IEC Guide 43:1984 | Development and operation of laboratory proficiency testing | ||||
| ISO/IEC Guide 43-2:1997 | Proficiency testing by interlaboratory comparisons -- Part 2: Selection and use of proficiency testing schemes by laboratory accreditation bodies | ||||
| ISO/IEC Guide 43-1:1997 | Proficiency testing by interlaboratory comparisons -- Part 1: Development and operation of proficiency testing schemes | ||||
| ISO/IEC Guide 53:1988 | An approach to the utilization of a supplier's quality system in third party product certification | ||||
| ISO/IEC Guide 53:2005 | Conformity assessment -- Guidance on the use of an organization's quality management system in product certification | ||||
| ISO/IEC Guide 57:1991 | Guidelines for the presentation of inspection results | ||||
| ISO/IEC Guide 60:1994 | ISO/IEC Code of good practice for conformity assessment | ||||
| ISO/CD 20069 | Change assessment of devices intended for administration of medicinal products | ||||
| ISO/IEC Guide 65:1996 | General requirements for bodies operating product certification systems | ||||
| ISO/IEC Guide 60:2004 | Conformity assessment -- Code of good practice | ||||
| ISO/IEC Guide 61:1996 | General requirements for assessment and accreditation of certification/registration bodies | ||||
| ISO/IEC Guide 68:2002 | Arrangements for the recognition and acceptance of conformity assessment results | ||||
| ISO/IEC Guide 67:2004 | Conformity assessment -- Fundamentals of product certification | ||||
| ISO/PAS 17003:2004 | Conformity assessment -- Complaints and appeals -- Principles and requirements | ||||
| ISO/PAS 17001:2005 | Conformity assessment -- Impartiality -- Principles and requirements | ||||
| ISO/PAS 17002:2004 | Conformity assessment -- Confidentiality -- Principles and requirements | ||||
| ISO/PAS 17004:2005 | Conformity assessment -- Disclosure of information -- Principles and requirements | ||||
| ISO/IEC 17007:2009 | Conformity assessment -- Guidance for drafting normative documents suitable for use for conformity assessment | ||||
| ISO/IEC TR 17010:1998 | General requirements for bodies providing accreditation of inspection bodies | ||||
| ISO/IEC 17011:2004 | Conformity assessment -- General requirements for accreditation bodies accrediting conformity assessment bodies | ||||
| ISO/PAS 17005:2008 | Conformity assessment -- Use of management systems -- Principles and requirements | ||||
| ISO 9355-2:1999 | Ergonomic requirements for the design of displays and control actuators -- Part 2: Displays | ||||
| ISO 7937:1985 | Microbiology -- General guidance for enumeration of Clostridium perfringens -- Colony-count technique | ||||
| ISO/IEC 17021-1:2015 | Conformity assessment -- Requirements for bodies providing audit and certification of management systems -- Part 1: Requirements | ||||
| ISO/IEC 17021-2:2016 | Conformity assessment -- Requirements for bodies providing audit and certification of management systems -- Part 2: Competence requirements for auditing and certification of environmental management systems | ||||
| ISO/IEC 17025:2005/Cor 1:2006 | |||||
| ISO/IEC 17030:2003 | Conformity assessment -- General requirements for third-party marks of conformity | ||||
| ISO/IEC 17040:2005 | Conformity assessment -- General requirements for peer assessment of conformity assessment bodies and accreditation bodies | ||||
| ISO/CD 20611 | Adventure tourism -- Sustainability good practices -- Requirements and recommendations | ||||
| ISO 6887:1983 | Microbiology -- General guidance for the preparation of dilutions for microbiological examination | ||||
| ISO 6888:1983 | Microbiology -- General guidance for enumeration of Staphylococcus aureus -- Colony count technique | ||||
| ISO 7667:1983 | Microbiology -- Standard layout for methods of microbiological examination | ||||
| ISO/AWI TR 13581 | Health Informatics - Guidance for maintenance of object identifiers OID | ||||
| ISO 7704:1985 | Water quality -- Evaluation of membrane filters used for microbiological analyses | ||||
| ISO 7899-1:1984 | Water quality -- Detection and enumeration of faecal streptococci -- Part 1: Method by enrichment in a liquid medium | ||||
| ISO 7899-1:1998 | Water quality -- Detection and enumeration of intestinal enterococci -- Part 1: Miniaturized method (Most Probable Number) for surface and waste water | ||||
| ISO/CD 8199 | Water quality -- General guidance on the enumeration of micro-organisms by culture | ||||
| ISO 9308-1:2000/Cor 1:2007 | |||||
| ISO 9308-1:2000 | Water quality -- Detection and enumeration of Escherichia coli and coliform bacteria -- Part 1: Membrane filtration method | ||||
| ISO 9308-1:2014/Amd 1:2016 | |||||
| ISO 9308-3:1998/Cor 1:2000 |
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