Can EU Device Regulation Go Any Quicker? We Doubt It

Medical device regulation is like a colander. It will catch most of what you want it to catch, but every so often a bit of spaghetti slips through the hole. A UK parliamentary committee has decided we must plug all the holes right away, which brings us to question the function of the thing in the first place.

This week’s View From The Med is online now, here. In it we discuss the proposed changed to EU device regulation in the context of a new report issued this week by the UK Government,s parliamentary select committee on science and technology. Two years after the recall of the first metal on metal hip, and almost a year after the PIP scandal broke, the committee is perhaps being a little audacious in calling for instant fixes to what are some institutionally ingrained practices. Root and branch regulatory infrastructure doesn’t come quickly or cheaply, so we’re wondering whether this is a bit of a poke in the ribs of the Eurocrats, or at very least the UK chaps wanting to show they’ve dispatched their duties and now it’s up to those useless Europeans!

Anyway, see what you think.

published: November 2, 2012 in: medlatest Editorial, Regulatory

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