European Commission jury still out over future legal framework for recast
This article was originally published in RAJ Devices
The European Commission is still keeping its options open on what legal framework to use in recasting the three medical device directives – the Medical Devices Directive (93/42/EEC), the Active Implantable Medical Device Directive (90/385/EEC) and the In Vitro Diagnostics Directive (98/79/EC).
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