from blood cell analysis

from blood cell analysis, Total:71 items.

The international standard classification for "from blood cell analysis" includes: Laboratory medicine , Medical Sciences and health care facilities in general , Biology. Botany. Zoology .

The Chinese standard classification for "from blood cell analysis" includes: Sanitation in general , Medical laboratory equipment , Basic Subject in general .

Professional Standard - Hygiene

WS/T 405-2012 Reference intervals for blood cell analysis
WS/T 347-2024 Guideline for the calibration of complete blood cell count
WS/T 360-2024 Guideline for enumeration of peripheral blood lymphocyte subsets by flow cytometry
WS 347-2011 Calibration Guide for Blood Cell Analysis
WS/T 347-2011 Guideline for the calibration of blood cell assays
WS/T 360-2011 Guidelines for peripheral lymphocyte subsets by flow cytometry
WS/T 779-2021 Reference intervals of blood cell analysis for children

National Health Commission of the People's Republic of China

WST 347:2011 Calibration Guide for Blood Cell Analysis
WST 360:2011 Guidelines for detection of peripheral blood lymphocyte subsets by flow cytometry

National Metrological Verification Regulations of the People's Republic of China

JJG 714-1990 Verification Regulation of Blood Cell Analyzer
JJG 714-2012 Verification Regulation of Blood Cell Analyzers

Professional Standard - Medicine

YY/T 0701-2008 Calibrator for hematology analyzer
YY/T 0456.2-2003 Regents for hematology analyzer use - Part 2: Hemolysin
YY/T 0702-2008 Control material for hematology analyzer
YY/T 0456.5-2014 Reagents for hematology analyzer―Part 5:Reticulocyte enumeration reagents
YY/T 0456.4-2014 Reagents for hematology analyzer―Part 4:Nucleated red blood cell enumeration reagents
YY/T 1452-2016 Dry hematology analyzer(centrifuge method)
YY/T 0456.1-2003 Regents for hematology analyzer use - Part 1: Rinse
YY/T 0456.3-2003 Regents for hematology analyzer use—Part 3:Diluent

Group Standards of the People's Republic of China

T/CSBT 009-2021 Technical guideline for genotyping of erythrocyte blood group
T/SHSYCXH 7-2022 Test method of human monocyte populations from peripheral blood-Flow cytometry
T/CSCB 0004-2021 Human hematopoietic stem/progenitor cell
T/CITS 143-2024 Requirements for blood cell analysis report
T/CEAC 038-2024 Serum-free cell culture medium

未注明发布机构

CLSI H26-A2-2010 Verification, Validation and Quality Assurance of Automated Hematology Analyzers
CLSI H43-A2-2007 Clinical Flow Cytometric Analysis of Neoplastic Hematolymphoid Cells; Approved Guideline—Second Edition
NCCLS H7-A3-2000 Procedure for determination of hematocrit by microhematocrit method

Professional Standard - Aquaculture

SC/T 7016.12-2012 Fish cell lines-Part 12:Carp leucocytes cell line(CLC)

Professional Standard - Agriculture

584药典化学药和生物制品卷-2010 Chapter VIII Drugs for Blood System Section 1 Drugs for Raising Blood Cells 2. Drugs for Raising Leukocytes Recombinant Human Granulocyte Macrophage Stimulating Factor
583药典化学药和生物制品卷-2010 Chapter VIII Drugs for Blood System Section 1 Drugs for Raising Blood Cells 2. Drugs for Raising Leukocytes Recombinant Human Granulocyte Stimulating Factor
582药典化学药和生物制品卷-2010 Chapter 8 Medications for Blood System Section 1 Drugs for Raising Blood Cells 2. Drugs for Raising White Blood Cells Likejun

German Institute for Standardization

DIN 58932-2:1998-06 Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
DIN 58932-2:1998 Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
DIN 58932-4:2003 Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
DIN EN ISO 20186-3:2018-02 Draft Document - Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Cellular RNA - Part 3: Isolated circulating cell free DNA from plasma (ISO/DIS 20186-3:2018); German and English version...
DIN 58932-3:2024 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrocytes; Text in German and English
DIN 58932-3:2023-07 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrocytes; Text in German and English / Note: Date of issue 2023-06-02*Intended as replacement for...
DIN 58932-3:2023 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrocytes; Text in German and English
DIN EN ISO 20186-3 E:2018 Draft Document - Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Cellular RNA - Part 3: Isolated circulating cell free DNA from plasma (ISO/DIS 20186-3:2018); German and English version...
DIN 58932-4:2003-07 Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
DIN CEN/TS 17742:2022-07 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma; German version CEN/TS 17742:2022
DIN CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma; German version CEN/TS 17742:2022
DIN 58932-3 E:2016 Draft Document - Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrozytes; Text in German and English
DIN 58932-6 E:2021-02 Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes
DIN 58932-6:2021-08 Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes; Text in German and English
DIN EN ISO 20186-3:2020-04 Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019); German version EN ISO 20186-3:2019
DIN 58932-6:2021-02 Draft Document - Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes; Text in German and English

Korean Agency for Technology and Standards (KATS)

KS P 4204-2021 Hemocytometer

Military Standards (MIL-STD)

DOD A-A-50802 A-1992 COUNTER, BLOOD CELLS, DIFFERENTIAL
DOD A-A-50825-1981 CHAMBER, COUNTING, BLOOD CELLS, HEMACYTOMETER

CZ-CSN

CSN 70 5228-1965 Hematocrit tube

British Standards Institution (BSI)

BS EN ISO 20186-3:2019 Molecular in-vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free DNA from plasma
BS PD CEN/TS 16835-3:2015 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood-Isolated circulating cell free DNA from plasma
BS PD CEN/TS 17742:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood. Isolated circulating cell free RNA from plasma
PD CEN/TS 17742:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood. Isolated circulating cell free RNA from plasma

European Committee for Standardization (CEN)

FprCEN/TS 17742-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
prEN ISO 18703 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma

Spanish Association for Standardization (UNE)

UNE-CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma (Endorsed by Asociación Española de Normalización in May of 2022.)

Danish Standards Foundation

DANSK DS/CEN/TS 17742:2022 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for venous whole blood – Isolated circulating cell free RNA from plasma

Standards Norway

SN-CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma

Ente Nazionale Italiano di Unificazione

UNI CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
UNI EN ISO 20186-3:2020 Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma
UNI CEN/TS 16835-3:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma

Canadian Standards Association (CSA)

CSA Z900.2.5-03 UPD 2-2007 Lymphohematopoietic Cells for Transplantation
CSA Z900.2.5-03-CAN/CSA UPD 2-2007 Lymphohematopoietic Cells for Transplantation
CSA Z900.2.5-03-2003 Lymphohematopoetic cells for transplantation
CAN/CSA-Z900.2.5-2017 Lymphohematopoietic cells for transplantation
CAN/CSA-Z900.2.5-2022 Lymphohematopoietic cells for transplantation
CAN/CSA-ISO 20186-3-2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma

Japanese Industrial Standards Committee (JISC)

JIS T 7326:1989 Hematocrit centrifuge