Full Description

This document provides guidance to manufacturers on the minimum requirements for the lifecyclemanagement of in vitro diagnostic (IVD) medical devices that are developed in preparation for and inresponse to a public health emergency involving infectious agents requiring immediate availability ofauthorized IVD devices.

NOTE: This document does not replace existing national (or regional) regulatory pathway requirements for IVD medical devices under non-emergency situations. The regulatory authorization process of emergency use-IVD medical devices is country-specific and it includes:

— following a risk management process;
— monitoring the device’s post-market performance and quality assurance;
— implementing a communication system.

Product Details

Published:

11/30/2024

ISBN(s):

9780539245929

Number of Pages:

22

File Size:

1 file , 1.5 MB

Note:

This product is restricted and cannot be purchased in the following countries Ukraine, Russia, Belarus