February 2009 – Cross and Cross Research SA are pleased to inform that up to now, they are compliant to the requirementsof the Italian Decree, 31st March 2008 “Definition of the minimum requirements which Contract Research Organisations (CROs) shall satisfy in order to work within clinical trials on medicinal products”.

Self-certification drawn up in compliance with the specific Determination by the General Director of AIFA, has been notified to the Italian Drug Agency. This certification is mandatory for perform, monitor or audit clinical studies performed in Italy.

This is a new step forward in the CROss Alliance quality accreditation strategy which may facilitates study registration procedures to our Sponsors in Italy who constantly rely on our services.