Iso Iec 17000 Y Del Vim

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  1. Iso Iec 17000 Y Del Vim 7
  2. Norma Iso/iec 17000 Y Del Vim

.ISO/IEC 17025 (2005) General requirements for the competence of testing and calibration laboratories. International Organization for Standardization/ International Electrotechnical Committee, Geneva.ISO 15189 (2012) Medical laboratories - Requirements for quality and competence.

International Organization for Standardization, Geneva.I. Papadakis and B. Magnusson (2010) Metrology in Chemistry and Traceability of Analytical Measurements. Wenclawiak, M.

Hadjicostas (Eds) Quality assurance in analytical chemistry, 2nd edn. Springer, Heidelberg, pp 201–213.ISO 9000 (2005) Quality management systems – fundamentals and vocabulary. International Organization for Standardization, Geneva.ISO/IEC Guide 99 (2007): International vocabulary of metrology - Basic and general concepts and associated terms (VIM 3rd edn). Available from.ISO/IEC 17000 (2004) Conformity assessment - Vocabulary and general principles. Abbondio vintage edition.

IsoIso Iec 17000 Y Del Vim

Iso Iec 17000 Y Del Vim 7

International Organization for Standardization/International Electrotechnical Committee, Geneva.Eurachem/CITAC Guide (2003) Traceability in Chemical Measurement. Available from.ILAC P 14:01 (2013) ILAC Policy for uncertainty in calibration. International Laboratory Accreditation Cooperation. Available from.ILAC-G24:2007 Guidelines for the determination of calibration intervals of measuring instruments. International Laboratory Accreditation Cooperation. Available from.Eurachem/CITAC Leaflet (2003) Metrological traceability of analytical results.

Iso iec 17000

Norma Iso/iec 17000 Y Del Vim

Available from.ISO/IEC 17011 (2004) Conformity assessment- General requirements for accreditation bodies accrediting conformity assessment bodies. International Organization for Standardization/ International Electrotechnical Committee, Geneva.ILAC P 10:01 (2013) ILAC Policy on traceability of measurement results. International Laboratory Accreditation Cooperation. Available from.ISO Guide 34 (2009) General requirements for the competence of reference materials producers. International Organization for Standardization/ International Electrotechnical Committee, Geneva.Directive 98/79/EC of the European Parliament and the Council Directive on in vitro diagnostic medical devices (1998) OJ L 331/1.K. Tsimillis, Accred. 20, 53 (2015).