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Homepage>BS Standards>01 GENERALITIES. TERMINOLOGY. STANDARDIZATION. DOCUMENTATION>01.040 Vocabularies>01.040.19 Testing (Vocabularies)>PD ISO/TS 17822-1:2014 <i>In</i> <i>vitro</i> diagnostic test systems. Qualitative nucleic acid-based <i>in</i> <i>vitro</i> examination procedures for detection and identification of microbial pathogens General requirements, terms and definitions
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PD ISO/TS 17822-1:2014 <i>In</i> <i>vitro</i> diagnostic test systems. Qualitative nucleic acid-based <i>in</i> <i>vitro</i> examination procedures for detection and identification of microbial pathogens General requirements, terms and definitions

PD ISO/TS 17822-1:2014

<i>In</i> <i>vitro</i> diagnostic test systems. Qualitative nucleic acid-based <i>in</i> <i>vitro</i> examination procedures for detection and identification of microbial pathogens General requirements, terms and definitions

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Standard number:PD ISO/TS 17822-1:2014
Pages:34
Released:2014-12-31
ISBN:978 0 580 89200 4
Status:Standard
DESCRIPTION

PD ISO/TS 17822-1:2014


This standard PD ISO/TS 17822-1:2014 In vitro diagnostic test systems. Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens is classified in these ICS categories:
  • 01.040.19 Testing (Vocabularies)
  • 11.100.01 Laboratory medicine in general

This Technical Specification is intended for

  • IVD medical device manufacturers, medical laboratories, and research and development laboratories that develop nucleic acid-based qualitative in vitro diagnostic examination procedures for the detection and identification of microbial pathogens in human specimens, and

  • medical laboratories that perform nucleic acid-based in vitro diagnostic examinations for the detection and identification of microbial pathogens in human specimens.

This part of ISO/TS 17822 does not apply to

  • nucleic acid-based examinations that are not intended for in vitro diagnostic use, or

  • quantitative nucleic acid-based in vitro diagnostic examination procedures.