MEDIMARK EUROPE

In our previous edition, we published a comprehensive glossary of revisions to Medical Device Directive 93/42/EEC and Active Implantable Medical Device Directive 90/385/EEC. In this issue, we focus on changes which may affect your currents labels and Instructions for Use (IFU). Knowing the delay for translation and printing, it is time to prepare your mandatory revisions which will become law on 21 March 2010.