dimarts, 7 de març del 2017

South Korean regulators clarify UDI, KGMP rules for medical devices

Emergo GroupBy Stewart Eisenhart, Emergo Group

The South Korean Ministry of Food and Drug Safety (MFDS) has issued clarifications on medical device registration and quality system requirements whose enforcement dates are imminent.

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 regulators clarify UDI, KGMP rules for medical devices appeared first on MassDevice.



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