Brussels, 22/10/2013 (Agence Europe) - On Tuesday 22 October, the European Parliament voted in favour of stricter monitoring and certification procedures to ensure full compliance and traceability of medical devices. MEPs also tightened up information and ethical requirements for diagnostic medical devices used for in vitro testing. Meeting up for their plenary meeting in Strasbourg, the European Parliament adopted the report by Dagmar Roth-Behrendt (S&D, Germany) on medical devices by 569...