
Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer
出版:International Organization for Standardization

专家解读视频
Specifies a process for manufacturers of in vitro diagnostic medical devices to validate quality control procedures they recommend to their users.
NEN ISO 15198:2004 - Identical
NBR NM-ISO 15198:2008 - Identical
BS ISO 15198:2004 - Identical
KS P ISO 15198:2006 - Identical
BS ISO 15198 : 2004 - Identical
DS ISO 15198 : 2004 - Identical
GOST R ISO 15198 : 2009 - Identical
NEN ISO 15198 : 2004 - Identical
NBR NM-ISO 15198 : 2008 ERRATA 2011 - Identical
NEN ISO 15198 : 2004 - Identical
BS ISO 15198 : 2004 - Identical
DS ISO 15198 : 2004 - Identical
NBR NM-ISO 15198 : 2008 ERRATA 2011 - Identical
GOST R ISO 15198 : 2009 - Identical