We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Report: Regulation of Device Reprocessing Fragmented in EU
Report: Regulation of Device Reprocessing Fragmented in EU
July 8, 2008
A new report by the European Commission (EC) paints a dim picture of regulation for reprocessing medical devices in the EU, calling the system fragmented and the practice poorly controlled.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor