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Construction requirements of health quarantine laboratory testing capability on entry-exit special goods
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Basic data
| Standard ID | SN/T 4610-2016 (SN/T4610-2016) |
| Description (Translated English) | Construction requirements of health quarantine laboratory testing capability on entry-exit special goods |
| Sector / Industry | Commodity Inspection Standard (Recommended) |
| Classification of Chinese Standard | C62 |
| Word Count Estimation | 6,619 |
| Date of Issue | 2016-08-23 |
| Date of Implementation | 2017-03-01 |
| Regulation (derived from) | State-Quality-Inspection-Certification (2016)438 |
| Issuing agency(ies) | General Administration of Customs |
SN/T 4610-2016: Construction requirements of health quarantine laboratory testing capability on entry-exit special goods
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Construction requirements of health quarantine laboratory testing capability on entry-exit special goods
People's Republic of China Exit Inspection and Quarantine standards
Entry and exit of special items health quarantine laboratories
Testing capacity building requirements
2016-08-23 released
2017-03-01 Implementation
People's Republic of China
General Administration of Quality Supervision, Inspection and Quarantine released
Exit Inspection and Quarantine of People's Republic of China
Industry Standard
Entry and exit of special items health quarantine laboratories
Testing capacity building requirements
China Standard Press
First edition of November.2017
Foreword
This standard was drafted in accordance with the rules given in GB/T 1.1-2009.
This standard is proposed and managed by the National Certification and Accreditation Administration Committee.
This standard was drafted by Zhejiang Entry-Exit Inspection and Quarantine of People's Republic of China, Shanghai Entry-Exit Inspection and Quarantine Bureau, People's Republic of China
Epidemic
The main drafters of this standard. Qi Runzi, Wu Zhonghua, Bai Jie, Lu Ye, Xu Feng, Yu Bin, Lou Yating, Zhao Liang, Ma Xiang.
Entry and exit of special items health quarantine laboratories
Testing capacity building requirements
1 Scope
This standard specifies the basic requirements for the inspection capacity of health and quarantine laboratories for special items of exit and entry.
This standard applies to the entry and exit of special items of health and quarantine laboratories planning, design, construction and assessment evaluation.
2 Normative references
The following documents for the application of this document is essential. For dated references, only the dated version applies to this article
Pieces. For undated references, the latest edition (including all amendments) applies to this document.
GB 19489 laboratory biosafety common requirements
GB 50346 Biosafety Laboratory Building Specifications
WS233 Microbiological and Biomedical Laboratory General Principles of Biosafety
Pathogenic microorganisms laboratory biosafety regulations (People's Republic of China State Council Decree No. 424)
Administration of Quality Supervision and Quarantine of the State Administration of Quality Supervision, Inspection and Quarantine (AQSIQ General Administration of Quality Supervision, Inspection and Quarantine)
ISO /IEC 17025 testing and calibration laboratory capacity requirements (Generalrequirementsforthecompetenceof
testingandcalibrationlaboratories)
3 laboratory testing
3.1 test object
Entry and exit of microorganisms, human tissues, biological products, blood and other products and other special items.
3.2 laboratory test items
In accordance with the provisions of the State Administration of Quality Supervision, Inspection and Quarantine on the entry and exit of special items of health quarantine, the implementation of risk assessment of special items in the process, according to special
Different types of items, special items contain or may contain the type of pathogenic microorganisms, the export of special items of biological or biological
Full control system, etc., to determine whether the need to carry out special items laboratory testing and laboratory testing needs to be carried out. Laboratory test
Test items should include (but not limited to) the following.
--- Medical microbiology, microbial identification of environmental microbiology;
--- Medical parasite detection and identification;
--- Environmental Microbial Agents ecological safety testing;
--- human tissue, blood and its products, biological products, infectious markers detection;
--- Detection of infectious disease markers in endemic or endemic areas of exporting countries or regions of special items;
--- Compliance testing;
--- biological risk factor test;
--- Genetic testing of human genetic resources;
...