DIN EN ISO 16256 - DRAFT PDF

Published Date: 02/01/2022

Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021)

Published Date: 03/01/2021

Draft Document - Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO/DIS 16256:2021); German and English version prEN ISO 16256:2021

Published Date: 04/01/2013

Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012)

Published Date: 09/01/2011

Draft Document - Clinical laboratory testing and in vitro diagnostic systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO/DIS 16256:2011); German version prEN ISO 16256:2011

Published Date: 10/01/2024

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)

Published Date: 04/01/2009

Draft Document - Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro test systems - Limulus amebocyte lysate (LAL) test (ISO/DIS 29701:2009); German version prEN ISO 29701:2009

Published Date: 10/01/2024

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

Published Date: 08/01/2024

Medical laboratories - Requirements for quality and competence (ISO 15189:2022)

Published Date: 05/01/1998