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Journal Article |
endingPage |
105 |
issn |
1433-6510 |
issueIdentifier |
3-4 |
pageRange |
86-105 |
publicationName |
Clinical laboratory |
startingPage |
86 |
bibliographicCitation |
Wood WG. Has the introduction of the European Parliament Directive 98/79/EC from 1998-10-27--concerning in-vitro diagnostic devices (IVD-directive) influenced performance of hormone immunoassay kits in terms of precision and accuracy? Results from selected external quality assessment (EQA) schemes between 1993 and 2008. Clin Lab. 2009;55(3-4):86–105. PMID: 19462931. |
creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8da2723a1bf7ab568b58f81640e2066f |
date |
2009 |
identifier |
https://pubmed.ncbi.nlm.nih.gov/19462931 |
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https://portal.issn.org/resource/ISSN/1433-6510 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21662 |
language |
English |
source |
https://pubmed.ncbi.nlm.nih.gov/ |
title |
Has the introduction of the European Parliament Directive 98/79/EC from 1998-10-27--concerning in-vitro diagnostic devices (IVD-directive) influenced performance of hormone immunoassay kits in terms of precision and accuracy? Results from selected external quality assessment (EQA) schemes between 1993 and 2008 |
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