After having contributed to the improvement of medical devices legislation in many ways over the years (most recently by helping the European Parliament to come up with an initiative for targeted amendments to the MDR) it is now my great honour to have been invited as external independent expert to assist the Bundestag (the German Parliament) in forming the MDR revision agenda that the German government should take to Brussels.
Why should we watch what happens in German Parliament?
The Council is [...]
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