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Can I read In vitro diagnostic test systems -- Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens -- Part 1: General requirements, terms and definitions on EtoBox?
In vitro diagnostic test systems -- Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens -- Part 1: General requirements, terms and definitions by ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems is a reference work available to read on EtoBox.
What is In vitro diagnostic test systems -- Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens -- Part 1: General requirements, terms and definitions about?
ISO/TS 17822-1:2014 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.
Who reads In vitro diagnostic test systems -- Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens -- Part 1: General requirements, terms and definitions?
It is typically read by working professionals who need an authoritative practice reference.
Common subject areas: medicine, law, business, engineering.
- Author
- ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems
- Publisher
- ISO
- Published
- 2014
- Language
- EN
- Category
- reference
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