European Commission highlights tissue and cell-related device problems in 2010-2012
This article was originally published in SRA
The European Commission has published a report on the EU Rapid Alert system for human Tissues and Cells (RATC) system during 2010-2012, which includes concerns relating to certain medical devices1.
You may also be interested in...
The European Commission has updated its rolling plan. It now looks as if current member state rules for non-medical products could persist beyond the 26 May 2021 deadline.
A formal notice ends the debate over the legality of making modules of the new Eudamed 3 medical device database available as soon as they are ready.
Notified bodies should now be regulated centrally in Europe rather than by individual EU member states. That is the view of one of Europe’s most experienced notified body experts.