CLSI I/LA29 A : 1ED 2008
|
DETECTION OF HLA-SPECIFIC ALLOANTIBODY BY FLOW CYTOMETRY AND SOLID PHASE ASSAYS |
CLSI POCT10 A2 : 2ED 2011
|
PHYSICIAN AND NONPHYSICIAN PROVIDER-PERFORMED MICROSCOPY TESTING |
CLSI M43 A : 1ED 2011
|
METHODS FOR ANTIMICROBIAL SUSCEPTIBILITY TESTING FOR HUMAN MYCOPLASMAS |
CLSI M54 A : 2012
|
PRINCIPLES AND PROCEDURES FOR DETECTION OF FUNGI IN CLINICAL SPECIMENS - DIRECT EXAMINATION AND CULTURE |
CLSI NBS02 A2 : 2ED 2013
|
NEWBORN SCREENING FOLLOW-UP |
CLSI AUTO3 A2 : 2ED 2009
|
LABORATORY AUTOMATION: COMMUNICATIONS WITH AUTOMATED CLINICAL LABORATORY SYSTEMS, INSTRUMENTS, DEVICES, AND INFORMATION SYSTEMS |
CLSI MM7 A2 : 2ED 2013
|
FLUORESCENCE IN SITU HYBRIDIZATION METHODS FOR CLINICAL LABORATORIES |
CLSI EP18 A2 : 2ED 2009
|
RISK MANAGEMENT TECHNIQUES TO IDENTIFY AND CONTROL LABORATORY ERROR SOURCES |
CLSI POCT11 A2 : 2ED 2011
|
PULSE OXIMETRY |
CLSI H42 A2 : 2ED 2007
|
ENUMERATION OF IMMUNOLOGICALLY DEFINED CELL POPULATIONS BY FLOW CYTOMETRY |
CLSI MM9 A2 : 2ED 2014
|
NUCLEIC ACID SEQUENCING METHODS IN DIAGNOSTIC LABORATORY MEDICINE |
CLSI M38 A2 : 2ED 2008
|
REFERENCE METHOD FOR BROTH DILUTION ANTIFUNGAL SUSCEPTIBILITY TESTING OF FILAMENTOUS FUNGI |
CLSI EP25 A : 1ED 2009
|
EVALUATION OF STABILITY OF IN VITRO DIAGNOSTIC REAGENTS |
CLSI EP26 A : 1ED 2013
|
USER EVALUATION OF BETWEEN-REAGENT LOT VARIATION |
CLSI H54 A : 1ED 2005
|
PROCEDURES FOR VALIDATION OF INR AND LOCAL CALIBRATION OF PT/INR SYSTEMS |
CLSI C52 A2 : 2ED 2007
|
TOXICOLOGY AND DRUG TESTING IN THE CLINICAL LABORATORY |
CLSI EP22 P : 1ED 2010
|
PRESENTATION OF A MANUFACTURER'S RISK MITIGATION INFORMATION FOR USERS OF IN VITRO DIAGNOSTIC DEVICES |
CLSI M11 A7 : 7ED 2007
|
METHODS FOR ANTIMICROBIAL SUSCEPTIBILITY TESTING OF ANAEROBIC BACTERIA |
CLSI H43 A2 : 2ED 2007
|
CLINICAL FLOW CYTOMETRIC ANALYSIS OF NEOPLASTIC HEMATOLYMPHOID CELLS |
CLSI MM18 A : 1ED 2008
|
INTERPRETIVE CRITERIA FOR IDENTIFICATION OF BACTERIA AND FUNGI BY DNA TARGET SEQUENCING |
CLSI C58 A : 1ED 2011
|
ASSESSMENT OF FETAL LUNG MATURITY BY THE LAMELLAR BODY COUNT |
CLSI H45 A2 : 2ED 2005
|
PERFORMANCE OF THE BLEEDING TIME TEST |
CLSI M45 A2 : 2ED 2010
|
METHODS FOR ANTIMICROBIAL DILUTION AND DISK SUSCEPTIBILITY TESTING OF INFREQUENTLY ISOLATED OR FASTIDIOUS BACTERIA |
BIS IS/ISO 15189 : 2012
|
MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE |
CLSI EP27 A : 1ED 2012
|
HOW TO CONSTRUCT AND INTERPRET AN ERROR GRID FOR QUANTITATIVE DIAGNOSTIC ASSAYS |
CLSI POCT4 A2 : 2ED 2006
|
POINT-OF-CARE IN VITRO DIAGNOSTIC (IVD) TESTING |
CLSI GP5 A3 : 3ED 2011
|
CLINICAL LABORATORY WASTE MANAGEMENT |
CLSI H60 A : 1ED 2014
|
LABORATORY TESTING FOR THE LUPUS ANTICOAGULANT |
I.S. EN ISO 15189:2012
|
MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE (ISO 15189:2012, CORRECTED VERSION 2014-08-15) |
CLSI NBS06 A : 1ED 2013
|
NEWBORN BLOOD SPOT SCREENING FOR SEVERE COMBINED IMMUNODEFICIENCY BY MEASUREMENT OF T-CELL RECEPTOR EXCISION CIRCLES |
CLSI POCT9 A : 1ED 2010
|
SELECTION CRITERIA FOR POINT-OF-CARE TESTING DEVICES |
CLSI MM1 A3 : 3ED 2012
|
MOLECULAR METHODS FOR CLINICAL GENETICS AND ONCOLOGY TESTING |
CLSI EP12 A2 : 2ED 2008
|
USER PROTOCOL FOR EVALUATION OF QUALITATIVE TEST PERFORMANCE |
CLSI M35 A2 : 2ED 2008
|
ABBREVIATED IDENTIFICATION OF BACTERIA AND YEAST |
CLSI NBS01 A6 : 6ED 2013
|
BLOOD COLLECTION ON FILTER PAPER FOR NEWBORN SCREENING PROGRAMS |
CLSI H21 A5 : 5ED 2008
|
COLLECTION, TRANSPORT, AND PROCESSING OF BLOOD SPECIMENS FOR TESTING PLASMA-BASED COAGULATION ASSAYS AND MOLECULAR HEMOSTASIS ASSAYS |
CLSI M11 A8 : 8ED 2012
|
METHODS FOR ANTIMICROBIAL SUSCEPTIBILITY TESTING OF ANAEROBIC BACTERIA |
CLSI I/LA28 A2 : 2ED 2011
|
QUALITY ASSURANCE FOR DESIGN CONTROL AND IMPLEMENTATION OF IMMUNOHISTOCHEMISTRY ASSAYS |
CLSI MM17 P : 1ED 2007
|
VERIFICATION AND VALIDATION OF MULTIPLEX NUCLEIC ACID ASSAYS |
CLSI NBS03 A : 1ED 2009
|
NEWBORN SCREENING FOR PRETERM, LOW BIRTH WEIGHT, AND SICK NEWBORNS |
CLSI C56 A : 1ED 2012
|
HEMOLYSIS, ICTERUS, AND LIPEMIA/TURBIDITY INDICES AS INDICATORS OF INTERFERENCE IN CLINICAL LABORATORY ANALYSIS |
CLSI MM13 A : 1ED 2006
|
COLLECTION, TRANSPORT, PREPARATION, AND STORAGE OF SPECIMENS FOR MOLECULAR METHODS |
CLSI I/LA2 A2 : 2ED 2006
|
QUALITY ASSURANCE OF LABORATORY TESTS FOR AUTOANTIBODIES TO NUCLEAR ANTIGENS: (1) INDIRECT FLUORESCENCE ASSAY FOR MICROSCOPY AND (2) MICROTITER ENZYME IMMUNOASSAY METHODS |
CLSI M44 A2 : 2ED 2009
|
METHOD FOR ANTIFUNGAL DISK DIFFUSION SUSCEPTIBILITY TESTING OF YEASTS
|
CLSI GP15 A3 : 3ED 2008
|
CERVICOVAGINAL CYTOLOGY BASED ON THE PAPANICOLAOU TECHNIQUE |
CLSI EP27 P : 1ED 2009
|
HOW TO CONSTRUCT AND INTERPRET AN ERROR GRID FOR DIAGNOSTIC ASSAYS |
CLSI POCT7 A : 1ED 2010
|
QUALITY MANAGEMENT: APPROACHES TO REDUCING ERRORS AT THE POINT OF CARE |
CLSI POCT8 A : 1ED 2010
|
QUALITY PRACTICES IN NONINSTRUMENTED POINT-OF-CARE TESTING: AN INSTRUCTIONAL MANUAL AND RESOURCES FOR HEALTH CARE WORKERS |
CLSI MM10 A : 1ED 2006
|
GENOTYPING FOR INFECTIOUS DISEASES: IDENTIFICATION AND CHARACTERIZATION |
CLSI EP17 A2 : 2ED 2012
|
EVALUATION OF DETECTION CAPABILITY FOR CLINICAL LABORATORY MEASUREMENT PROCEDURES |
PREN ISO 15189 : DRAFT 2011
|
MEDICAL LABORATORIES - PARTICULAR REQUIREMENTS FOR QUALITY AND COMPETENCE |
UNE-EN ISO 15189:2013
|
Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15) |
CLSI AUTO2 A2 : 2ED 2005
|
LABORATORY AUTOMATION: BAR CODES FOR SPECIMEN CONTAINER IDENTIFICATION |
CLSI M48 A : 1ED 2008
|
LABORATORY DETECTION AND IDENTIFICATION OF MYCOBACTERIA |
CLSI GP34 P : 1ED 2009
|
VALIDATION AND VERIFICATION OF TUBES FOR VENOUS AND CAPILLARY BLOOD SPECIMEN COLLECTION |
CLSI POCT7 P : 1ED 2009
|
QUALITY MANAGEMENT: APPROACHES TO REDUCING ERRORS AT THE POINT OF CARE |
CLSI MM5 A2 : 2ED 2012
|
NUCLEIC ACID AMPLIFICATION ASSAYS FOR MOLECULAR HEMATOPATHOLOGY |
CLSI EP23 A : 1ED 2011
|
LABORATORY QUALITY CONTROL BASED ON RISK MANAGEMENT |
CLSI GP2 A5 : 5ED 2006
|
LABORATORY DOCUMENTS - DEVELOPMENT AND CONTROL |
CLSI M41 A : 1ED 2006
|
VIRAL CULTURE |
CLSI POCT9 P : 1ED 2009
|
SELECTION CRITERIA FOR POINT-OF-CARE TESTING DEVICES |
CLSI MM13 P : 1ED 2005
|
COLLECTION, TRANSPORT, PREPARATION, AND STORAGE OF SPECIMENS FOR MOLECULAR METHODS |
CLSI EP30 A : 1ED 2010
|
CHARACTERIZATION AND QUALIFICATION OF COMMUTABLE REFERENCE MATERIALS FOR LABORATORY MEDICINE |
CLSI I/LA34 P : 1ED 2010
|
DESIGN AND VALIDATION OF IMMUNOASSAYS FOR ASSESSMENT OF HUMAN ALLERGENICITY OF NEW BIOTHERAPEUTIC DRUGS |
CLSI MM6 A2 : 2ED 2010
|
QUANTITATIVE MOLECULAR METHODS FOR INFECTIOUS DISEASES |
CLSI M2 A10 : 10ED 2008
|
PERFORMANCE STANDARDS FOR ANTIMICROBIAL DISK SUSCEPTIBILITY TESTS |
CLSI M7 A7 : 7ED 2006
|
METHODS FOR DILUTION ANTIMICROBIAL SUSCEPTIBILITY TESTS FOR BACTERIA THAT GROW AEROBICALLY |
CLSI NBS04 A : 1ED 2010
|
NEWBORN SCREENING BY TANDEM MASS SPECTROMETRY
|
CLSI C34 A3 : 3ED 2009
|
SWEAT TESTING: SAMPLE COLLECTION AND QUANTITATIVE CHLORIDE ANALYSIS |
CLSI NBS01 A5 : 5ED 2007
|
BLOOD COLLECTION ON FILTER PAPER FOR NEWBORN SCREENING PROGRAMS |
CLSI GP44 A4 : 4ED 2010
|
PROCEDURES FOR THE HANDLING AND PROCESSING OF BLOOD SPECIMENS FOR COMMON LABORATORY TESTS |
CLSI MM17 A : 1ED 2008
|
VERIFICATION AND VALIDATION OF MULTIPLEX NUCLEIC ACID ASSAYS |
CLSI H52 A2 : 2ED 2014
|
Red Blood Cell Diagnostic Testing Using Flow Cytometry; Approved Guideline—Second Edition |
CLSI VET01 A4 : 4ED 2013
|
PERFORMANCE STANDARDS FOR ANTIMICROBIAL DISK AND DILUTION SUSCEPTIBILITY TESTS FOR BACTERIA ISOLATED FROM ANIMALS |
DIN EN ISO 15189:2014-11
|
Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15) |
UNI EN ISO 15189 : 2013
|
MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE |
CLSI H20 A2 : 2ED 2007
|
Reference Leukocyte (WBC) Differential Count (Proportional) and Evaluation of Instrumental Methods, 2nd Edition
|
CLSI GP16-A3 : 2009
|
Urinalysis; Approved Guideline—Third Edition |
CLSI M39 A4 : 4ED 2014
|
ANALYSIS AND PRESENTATION OF CUMULATIVE ANTIMICROBIAL SUSCEPTIBILITY TEST DATA |
CLSI I/LA34 A : 1ED 2011
|
DESIGN AND VALIDATION OF IMMUNOASSAYS FOR ASSESSMENT OF HUMAN ALLERGENICITY OF NEW BIOTHERAPEUTIC DRUGS |
CLSI EP31 A : 1ED 2008
|
VERIFICATION OF COMPARABILITY OF PATIENT RESULTS WITHIN ONE HEALTH CARE SYSTEM |
CLSI NBS05 A : 1ED 2011
|
NEWBORN SCREENING FOR CYSTIC FIBROSIS |
CLSI C24 A3 : 3ED 2006
|
STATISTICAL QUALITY CONTROL FOR QUANTITATIVE MEASUREMENT PROCEDURES: PRINCIPLES AND DEFINITIONS |
CLSI EP24 A2 : 2ED 2011
|
ASSESSMENT OF THE DIAGNOSTIC ACCURACY OF LABORATORY TESTS USING RECEIVER OPERATING CHARACTERISTIC CURVES |
CLSI M7 A8 : 8ED 2008
|
METHODS FOR DILUTION ANTIMICROBIAL SUSCEPTIBILITY TESTS FOR BACTERIA THAT GROW AEROBICALLY |
CLSI H59 P : 1ED 2010
|
QUANTITATIVE D-DIMER FOR THE EXCLUSION OF VENOUS THROMBOEMBOLIC DISEASE |
CLSI QMS04 A2 : 2ED 2007
|
LABORATORY DESIGN |
CLSI H26 A2 : 2ED 2010
|
VALIDATION, VERIFICATION, AND QUALITY ASSURANCE OF AUTOMATED HEMATOLOGY ANALYZERS |
CLSI I/LA30 P : 1ED 2007
|
IMMUNOASSAY INTERFERENCE BY ENDOGENOUS ANTIBODIES |
CLSI MM10 P : 1ED 2005
|
GENOTYPING FOR INFECTIOUS DISEASES: IDENTIFICATION AND CHARACTERIZATION |
CLSI I/LA21 A2 : 2ED 2008
|
CLINICAL EVALUATION OF IMMUNOASSAYS |
CLSI MM18 P : 1ED 2007
|
INTERPRETIVE CRITERIA FOR MICROORGANISM IDENTIFICATION BY DNA TARGET SEQUENCING
|
CLSI MM1 A2 : 2ED 2006
|
MOLECULAR DIAGNOSTIC METHODS FOR GENETIC DISEASES |
CLSI MM22 A : 1ED 2014
|
MICROARRAYS FOR DIAGNOSIS AND MONITORING OF INFECTIOUS DISEASES |
CLSI H47 A2 : 2ED 2008
|
ONE-STAGE PROTHROMBIN TIME (PT) TEST AND ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT) TEST |
CLSI I/LA31 P : 1ED 2008
|
NEWBORN SCREENING GUIDELINES FOR PREMATURE AND/OR SICK NEWBORNS
|
CLSI M27 S3 : 3ED 2008
|
REFERENCE METHOD FOR BROTH DILUTION ANTIFUNGAL SUSCEPTIBILITY TESTING OF YEASTS |
CLSI I/LA32 P : 1ED 2009
|
NEWBORN SCREENING BY TANDEM MASS SPECTROMETRY |
CLSI MM20 A : 1ED 2012
|
QUALITY MANAGEMENT FOR MOLECULAR GENETIC TESTING |
CLSI MM11 A : 1ED 2007
|
MOLECULAR METHODS FOR BACTERIAL STRAIN TYPING |
CLSI POCT5 P : 1ED 2008
|
PERFORMANCE METRICS FOR CONTINUOUS INTERSTITIAL GLUCOSE MONITORING |
CLSI MM11 P : 1ED 2006
|
MOLECULAR METHODS FOR BACTERIAL STRAIN TYPING |
CLSI I/LA33 A : 1ED 2009
|
VALIDATION OF AUTOMATED SYSTEMS FOR IMMUNOHEMATOLOGICAL TESTING BEFORE IMPLEMENTATION |
11/30173018 DC : 0
|
BS EN ISO 15189 - MEDICAL LABORATORIES - PARTICULAR REQUIREMENTS FOR QUALITY AND COMPETENCE |
CLSI C53 P : 1ED 2008
|
CHARACTERIZATION AND QUALIFICATION OF COMMUTABLE REFERENCE MATERIALS FOR LABORATORY MEDICINE |
CLSI H58 AE : 1ED 2008
|
PLATELET FUNCTION TESTING BY AGGREGOMETRY |
CLSI EP28 A3 : 3ED 2010
|
DEFINING, ESTABLISHING, AND VERIFYING REFERENCE INTERVALS IN THE CLINICAL LABORATORY |
CLSI MM19 A : 1ED 2011
|
ESTABLISHING MOLECULAR TESTING IN CLINICAL LABORATORY ENVIRONMENTS |
CLSI I/LA25 A2 : 2011
|
MATERNAL SERUM SCREENING |
ISO 15189:2012
|
Medical laboratories — Requirements for quality and competence |
BS EN ISO 15189:2012
|
Medical laboratories. Requirements for quality and competence |
CLSI QMS01 A4 : 4ED 2011
|
QUALITY MANAGEMENT SYSTEM: A MODEL FOR LABORATORY SERVICES |
CLSI POCT13 A2 : 2ED 2005
|
GLUCOSE MONITORING IN SETTINGS WITHOUT LABORATORY SUPPORT |
CLSI I/LA20 A2 : 2ED 2009
|
ANALYTICAL PERFORMANCE CHARACTERISTICS AND CLINICAL UTILITY OF IMMUNOLOGICAL ASSAYS FOR HUMAN IMMUNOGLOBULIN E (IGE) ANTIBODIES AND DEFINED ALLERGEN SPECIFICITIES |
CLSI EP18 P2 : 2ED 2007
|
RISK MANAGEMENT TECHNIQUES TO IDENTIFY AND CONTROL LABORATORY ERROR SOURCES |
CLSI M28 A2 : 2ED 2005
|
PROCEDURES FOR THE RECOVERY AND IDENTIFICATION OF PARASITES FROM THE INTESTINAL TRACT |
CLSI I/LA30 A : 1ED 2008
|
IMMUNOASSAY INTERFERENCE BY ENDOGENOUS ANTIBODIES |
CLSI GP39 A6 : 6ED 2010
|
TUBES AND ADDITIVES FOR VENOUS AND CAPILLARY BLOOD SPECIMEN COLLECTION |
CLSI GP34 A : 1ED 2010
|
VALIDATION AND VERIFICATION OF TUBES FOR VENOUS AND CAPILLARY BLOOD SPECIMEN COLLECTION |
CLSI M41 P : 1ED 2006
|
VIRAL CULTURE |
CLSI POCT5 A : 1ED 2008
|
PERFORMANCE METRICS FOR CONTINUOUS INTERSTITIAL GLUCOSE MONITORING |
CLSI H59 A : 1ED 2011
|
QUANTITATIVE D-DIMER FOR THE EXCLUSION OF VENOUS THROMBOEMBOLIC DISEASE |
CLSI MM19 P : 1ED 2011
|
ESTABLISHING MOLECULAR TESTING IN CLINICAL LABORATORY ENVIRONMENTS |
CLSI M47 A : 1ED 2007
|
PRINCIPLES AND PROCEDURES FOR BLOOD CULTURES |
CLSI VET05 R : 1ED 2011
|
GENERATION, PRESENTATION, AND APPLICATION OF ANTIMICROBIAL SUSCEPTIBILITY TEST DATA FOR BACTERIA OF ANIMAL ORIGIN |
CLSI C49 A : 1ED 2007
|
ANALYSIS OF BODY FLUIDS IN CLINICAL CHEMISTRY |
CLSI C40 A2 : 2ED 2013
|
MEASUREMENT PROCEDURES FOR THE DETERMINATION OF LEAD CONCENTRATIONS IN BLOOD AND URINE |
CLSI M27 A3 : 3ED 2008
|
REFERENCE METHOD FOR BROTH DILUTION ANTIFUNGAL SUSCEPTIBILITY TESTING OF YEASTS |
CLSI GP41 A6 : 6ED 2007
|
PROCEDURES FOR THE COLLECTION OF DIAGNOSTIC BLOOD SPECIMENS BY VENIPUNCTURE |
CLSI M53 A : 1ED 2011
|
CRITERIA FOR LABORATORY TESTING AND DIAGNOSIS OF HUMAN IMMUNODEFICIENCY VIRUS INFECTION |
CLSI M51 A : 1ED 2010
|
METHOD FOR ANTIFUNGAL DISK DIFFUSION SUSCEPTIBILITY TESTING OF NONDERMATOPHYTE FILAMENTOUS FUNGI |
CLSI EP9 A3 : 3ED 2013
|
MEASUREMENT PROCEDURE COMPARISON AND BIAS ESTIMATION USING PATIENT SAMPLES |
CLSI MM16 A : 1ED 2006
|
USE OF EXTERNAL RNA CONTROLS IN GENE EXPRESSION ASSAYS |
CLSI POCT8 P : 1ED 2009
|
QUALITY PRACTICES IN NON-INSTRUMENTED NEAR-PATIENT TESTING: AN INSTRUCTIONAL MANUAL AND RESOURCES FOR HEALTH CARE WORKERS |
CLSI H2 A5 : 5ED 2011
|
PROCEDURES FOR THE ERYTHROCYTE SEDIMENTATION RATE TEST |
CLSI M53 P : 1ED 2010
|
CRITERIA FOR LABORATORY TESTING AND DIAGNOSIS OF HIV INFECTION |
CLSI M39 A3 : 3ED 2009
|
ANALYSIS AND PRESENTATION OF CUMULATIVE ANTIMICROBIAL SUSCEPTIBILITY TEST DATA |
CLSI VET02 A3 : 3ED 2008
|
DEVELOPMENT OF IN VITRO SUSCEPTIBILITY TESTING CRITERIA AND QUALITY CONTROL PARAMETERS FOR VETERINARY ANTIMICROBIAL AGENTS |
CLSI GP42 A6 : 6ED 2008
|
PROCEDURES AND DEVICES FOR THE COLLECTION OF DIAGNOSTIC CAPILLARY BLOOD SPECIMENS |
CLSI I/LA33 P : 1ED 2009
|
VALIDATION OF AUTOMATED DEVICES FOR IMMUNOHEMATOLOGIC TESTING PRIOR TO IMPLEMENTATION |
CLSI M2 A9 : 9ED 2006
|
PERFORMANCE STANDARDS FOR ANTIMICROBIAL DISK SUSCEPTIBILITY TESTS |
CLSI M24 A2 : 2ED 2011
|
SUSCEPTIBILITY TESTING OF MYCOBACTERIA, NOCARDIAE, AND OTHER AEROBIC ACTINOMYCETES |
CLSI M47 P : 1ED 2006
|
PRINCIPLES AND PROCEDURES FOR BLOOD CULTURES |
CLSI M50 P : 1ED 2008
|
QUALITY CONTROL FOR COMMERCIAL MICROBIAL IDENTIFICATION SYSTEMS |
CLSI GP17 A3 : 3ED 2012
|
CLINICAL LABORATORY SAFETY |
CLSI GP31 A : 1ED 2009
|
LABORATORY INSTRUMENT IMPLEMENTATION, VERIFICATION, AND MAINTENANCE |
CLSI POCT12 A3 : 3ED 2013
|
Point-of-Care Blood Glucose Testing in Acute and Chronic Care Facilities; Approved Guideline—Third Edition
|
CLSI C43 A2 : 2ED 2010
|
GAS CHROMATOGRAPHY/MASS SPECTROMETRY CONFIRMATION OF DRUGS |
CLSI I/LA26 A2 : 2ED 2013
|
PERFORMANCE OF SINGLE CELL IMMUNE RESPONSE ASSAYS |
CLSI C46 A2 : 2ED 2009
|
BLOOD GAS AND PH ANALYSIS AND RELATED MEASUREMENTS |