South Korean medical device regulators to align quality requirements with ISO 13485:2016

By Stewart Eisenhart, Emergo Group The South Korean Ministry of Food and Drug Safety (MFDS) has issued draft plans to align Korea Good Manufacturing Practice (KGMP) more closely to the ISO 13485:2016 medical device quality system standard. Get the full story here at the Emergo Group’s blog. The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees. The post South Korean medical device regulators to align quality requirements with ISO 13485:2016 appeared first on MassDevice.
Source: Mass Device - Category: Medical Devices Authors: Tags: Blog Emergo Group Source Type: news