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[1] ISO/IEC Guide 28:20047) , Conformity assessment — Guidance on a third-party certification system for products [src] [rss]

[2] ISO 9001:20088) , Quality management systems — Requirements [src] [rss]

[3] ISO 15189:20129) , Medical laboratories — Requirements for quality and competence [src] [rss]

[4] ISO/IEC 17000:200410) , Conformity assessment — Vocabulary and general principles [src] [rss]

[5] ISO/IEC 17020:2012, Conformity assessment — Requirements for the operation of various types of bodies performing inspection [src] [obp] [rss]

[6] ISO/IEC 17025:200511) , General requirements for the competence of testing and calibration laboratories [src] [rss]

[7] ISO/IEC 17030:200312) , Conformity assessment — General requirements for third-party marks of conformity [src] [rss]

[8] ISO/IEC 17065:2012, Conformity assessment — Requirements for bodies certifying products, processes and services [src] [obp] [rss]

[9] ISO/IEC 17067:2013, Conformity assessment — Fundamentals of product certification and guidelines for product certification schemes [src] [obp] [rss]

[10] OIML G 14:2011, Density measurement

[11] OIML R 79:2015, Labelling requirements for prepackages

[12] OIML R 87:2016, Quantity of product in prepackages