ISO/AWI TS 24883
Lateral flow immunoassay for rapid diagnostic testing — General guideline for test performance
Reference number
ISO/AWI TS 24883
Edition 1
Working draft
ISO/AWI TS 24883
88356
A working group has prepared a draft.

Abstract

This document provides the general principles and guideline for the rapid diagnostic testing (RDT) of LFIA used for the In vitro diagnostics as follows: — Design and development of LFIA — General guideline for test performance of LFIA — Recommendations for the use of LFIA This document is specific to the RDT of LFIA, which employ the gold nanoparticle as the conjugate and read the signal either with naked eye or through reader devices. This document does not apply to other types of LFIA such as automatic devices and microfluidic chips. This document should be expected to be helpful to increase efficiency and reduce trials and errors when manufacturing LFIA RDT products to the industries and/or manufacturers.

General information

  •  : Under development
    : New project registered in TC/SC work programme [20.00]
  •  : 1
  • ISO/TC 212
  • RSS updates

Got a question?

Check out our FAQs

Customer care
+41 22 749 08 88

Opening hours:
Monday to Friday - 09:00-12:00, 14:00-17:00 (UTC+1)