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vitro scopethis standard reference measurement procedures reference measurement program documents standard applies vitro pollutants emission impurities-gas chromatographic method scopethis standard basic part top groove
GB/T 19702-2005 in English

GB/T 19702-2005 in English

SUPERSEDED

In vitro

  • Issued on:2005-03-23
  • Implemented on:2005-12-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $180.00
$175.00
Standard No: GB/T 19702-2005
Document status: SUPERSEDED
Superseded by: GB/T 19702-2021 In vitro diagnostic medical devices -- Measurement of quantities in samples of biological origin -- Requirements for content and presentation of reference measurement procedures
Superseded on: 2022-04-01
Title in English: In vitro
Title in Chinese: 体外诊断医疗器械 生物源性样本中量的测量 参考测量程序的说明
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 business days
Issued on: 2005-03-23
Implemented on: 2005-12-01
ICS Classification: 11.040-Medical equipment
Chinese Classification: C30-Medical apparatus and devices in general
Professional Classification: GB-National Standard
Related Keywords: vitro scopethis standard
reference measurement procedures
reference measurement program documents
standard applies
vitro
Related Topics: biological source
UV solid sample volume
-19702
Microbial Diagnosis in Vitro Diagnostics
measurement
how to measure solid
Reference method for in vitro diagnostics
reference measurement
Sequencing sample size
In Vitro Diagnostic Medical Devices
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Sequencing data volume + sample volume
How to explain non-medical devices
Solid UV sample volume
gb19702
GB t 19702 2005
Biological samples semi-quantitative
GBT19702
GB/T 19702-2005
GB/T 19702-2021
In vitro diagnostic medical devices - measurement of quantities in samples of biological origin
Diagnostic test sample size formula
GBT 19703-2020: Certified reference materials and supporting documents for measurement of amounts of biogenic samples in in vitro diagnostic medical devices
gbt19702
gb/t 19702

《GB/T 19702-2005体外诊断医疗器械 生物源性样品中量的测量 参考测量程序的说明》由TC136(全国医用临床检验实验室和体外诊断系统标准化技术委员会)归口,主管部门为国家药品监督管理局
本标准规定了起草参考测量程序的要求。本标准适用于实验医学各个学科分支中,需要进行参考测量程序文件制作的所有个人、机构或研究所。


Scope

This standard specifies the requirements for drafting reference measurement procedures. This standard applies to all individuals, institutions or research institutes that need to make reference measurement program documents in various branches of experimental medicine.

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