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This document adopts ISO 14971:2019, which specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The process described in this document intends to assist manufacturers of medical devices to identify the hazards associated with the medical device, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls.

Product Details

Edition:

1st

Published:

06/26/2020

ISBN(s):

9781760729141

Number of Pages:

37

File Size:

1 file , 2.3 MB

Product Code(s):

10184366, 10184367, 10184368

Note:

This product is unavailable in Ukraine, Russia, Belarus