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18 - 22 October 2021
Virtual EventDelivered in CEST time zone

Daniele Bollati
Product Conformity Assessment at IMQ


Master's Degree in Biomolecular and Industrial Biotechnology at the University of Turin (Italy), several years of hand-on and R&D experience on non-active medical devices in the dental and orthopedic sector for an Italian company (Nobil Bio Ricerche). For the same company, laboratory activities for the development of specific methods for biomaterial characterization and biocompatibility evaluation and setting-up of clinical investigations and post-market clinical studies. Since 2015, he carries out activities of assessing the conformity of medical devices (technical file evaluation and on-site audit). Currently he works on behalf of the IMQ SpA Notified Body with the role of Product Assessor and Technical Expert on non-active medical devices. He's also actively collaborating on the development of adequate chemical-physical and biological tests for medical devices with CSI S.p.A. laboratory (part of the IMQ group).

Agenda Sessions

  • Substance-Based Medical Devices and How to Interpret EU MDR Requirements

    On Demand