Originally published as Covington E-Alert on September 26, 2012
Today the European Commission published its long awaited proposals for the revision of the EU regulatory framework for medical devices. Three Directives, i.e., Directive 90/385/EEC on active implantable medical devices, Directive 93/42/EEC on medical devices and Directive 98/79/EC on in vitro
Continue Reading New Medical Devices Regulations in the EU – Significant Changes But No Big Bang
