As a regulatory review board for medical device to be used by European, I hope they do as mentioned here even though it isn't in their mission statement and that was my argument with you, as it means they can approve not efficient medical device just based on safety without any evidence that it works.
https://crstodayeurope.com/articles/2015-feb/ce-mark-versus-fda-approval-which-system-has-it-right/
TechKnow Sydney, page-254
Currently unlisted. Proposed listing date: 4 SEPTEMBER 2024 #
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