The essential list of guidances for software medical devices
By Mitch on Wednesday, 22 February 2012, 09:21 - Regulations - Permalink
Too many documents in too many places, that’s what I felt the first time I
looked for guidances and other similar stuff about software medical
devices.
Where do I find relevant documents?
Which one do I begin with?
My answer:
I created a page where I gather my own list of guidances. It’s a selection of
guidances and recommendations for CE mark.
Hope you enjoy it :-)
