'Beyond compliance' can add strength to EU medical device regulation
This article was originally published in SRA
Executive Summary
The tools for proper and sound regulation of medical devices in the EU are all available, they simply need to be implemented fully. That is the consensus among users of the EU regulatory system, and it is the growing sentiment of those who, needs must, have had to become familiar with the sector, for political and other reasons, in the last 12-18 months.