BIS IS/ISO 15189 : 2012
|
MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE |
I.S. EN ISO 15189:2012
|
MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE (ISO 15189:2012, CORRECTED VERSION 2014-08-15) |
CLSI EP14 A3 : 2014
|
EVALUATION OF COMMUTABILITY OF PROCESSED SAMPLES |
PREN ISO 15189 : DRAFT 2011
|
MEDICAL LABORATORIES - PARTICULAR REQUIREMENTS FOR QUALITY AND COMPETENCE |
UNE-EN ISO 18113-1:2012
|
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009) |
UNE-EN ISO 15189:2013
|
Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15) |
CLSI EP30 A : 1ED 2010
|
CHARACTERIZATION AND QUALIFICATION OF COMMUTABLE REFERENCE MATERIALS FOR LABORATORY MEDICINE |
PD ISO Guide 34:2009
|
General requirements for the competence of reference material producers |
ISO Guide 34:2009
|
General requirements for the competence of reference material producers |
EN ISO 18113-1:2011
|
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009) |
UNI EN ISO 15189 : 2013
|
MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE |
CLSI EP31 A : 1ED 2008
|
VERIFICATION OF COMPARABILITY OF PATIENT RESULTS WITHIN ONE HEALTH CARE SYSTEM |
CLSI C28 P3 : 3ED 2008
|
DEFINING, ESTABLISHING, AND VERIFYING REFERENCE INTERVALS IN THE CLINICAL LABORATORY |
CLSI I/LA21 A2 : 2ED 2008
|
CLINICAL EVALUATION OF IMMUNOASSAYS |
CLSI C57 : 1ED 2015
|
MASS SPECTROMETRY FOR ANDROGEN AND ESTROGEN MEASUREMENTS IN SERUM |
CLSI H47 A2 : 2ED 2008
|
ONE-STAGE PROTHROMBIN TIME (PT) TEST AND ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT) TEST |
CLSI POCT6 : 1ED 2015
|
EFFECTS OF DIFFERENT SAMPLE TYPES ON GLUCOSE MEASUREMENTS |
11/30173018 DC : 0
|
BS EN ISO 15189 - MEDICAL LABORATORIES - PARTICULAR REQUIREMENTS FOR QUALITY AND COMPETENCE |
I.S. EN ISO 18113-1:2011
|
IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 1: TERMS, DEFINITIONS AND GENERAL REQUIREMENTS (ISO 18113-1:2009) |
CLSI C53 P : 1ED 2008
|
CHARACTERIZATION AND QUALIFICATION OF COMMUTABLE REFERENCE MATERIALS FOR LABORATORY MEDICINE |
CLSI EP28 A3 : 3ED 2010
|
DEFINING, ESTABLISHING, AND VERIFYING REFERENCE INTERVALS IN THE CLINICAL LABORATORY |
ISO 15189:2012
|
Medical laboratories — Requirements for quality and competence |
ISO 18113-1:2009
|
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements |
BS EN ISO 15189:2012
|
Medical laboratories. Requirements for quality and competence |
CLSI C49 A : 1ED 2007
|
ANALYSIS OF BODY FLUIDS IN CLINICAL CHEMISTRY |
DIN EN ISO 18113-1:2013-01
|
IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 1: TERMS, DEFINITIONS AND GENERAL REQUIREMENTS (ISO 18113-1:2009) |
BS EN ISO 18113-1:2011
|
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) Terms, definitions and general requirements |
UNI EN ISO 18113-1 : 2012
|
IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 1: TERMS, DEFINITIONS AND GENERAL REQUIREMENTS |