WARNING: We do not support Internet Explorer. It is not secure and will not work correctly. Please come back using a newer web browser.


In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens

CLSI ISO/TS 17822

In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens

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 document is available in electronic format only. 

List Price:
Log in/sign up to see price and add to cart

Details

Date of Publication: January 1, 2014

Order Code PDF: CLSI ISOTS17822E

Order Code Print: print not available

Edition: First

Pages: 22

CLSI ISO/TS 17822 Additional Details

Membership discounts cannot be applied to ISO documents because they are not published by CLSI. CLSI is able to offer ISO Technical Committee 212 approved and draft standards through an agreement with the American National Standards Institute.

Technical Committee: ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems