The Commission has launched a public consultation and a call for evidence on the EU’s legislation on medical devices and in vitro diagnostic medical devices, as part of the targeted evaluation of these rules.
The consultation provides stakeholders with the opportunity to express their views on how the current rules are performing and to highlight possible shortcomings.
The Regulations on medical devices and in vitro diagnostics aim to ensure that only safe and effective devices are available on the market, while supporting a competitive and innovative industry in this field…
