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- [3] 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 CLINICAL LABORATORY, 2009, 55 (3-4) : 86 - 105
- [4] Sigma metrics for assessing the analytical quality of the new multi-test VITROS® XT chemistry products slides11*For presentation and demonstration purposes only. VITROS XT Slides are currently under development and are not available to the public or for sale until approved under the requirements of the DIRECTIVE 98/79/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 27 October 1998 on in vitro diagnostic medical devices and the respective regulatory requirements of the target market CLINICA CHIMICA ACTA, 2019, 493 : S503 - S504