Dr. Maurizio Suppo, graduated as a molecular biologist, has +30 years of experience in Quality & Regulatory in international medical device and in-vitro diagnostic industry.
He has been the Director of EDMA (European Association of In-Vitro Diagnostic Manufacturers) from 95 to 98 and in those years, he has played a fundamental role in the drafting process of the EU IVD-Directive (98/79/EC) by representing the IVD industry at the EU Commission, EU Parliament and EU Council.
He has been responsible world-wide for RAQS/EHS for Dade Behring and later for Siemens Healthcare Diagnostics.
Dr. Suppo joined QARAD (www.qarad.com
) on July 2012 as principal consultant and became company co-owner on January 2016. QARAD is a leading European company specialized in RAQS consultancy for medical devices and IVDs.
Dr. Suppo is a trained auditor in ISO-9001, 13485 and MDSAP.