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MedTech Summit
Hybrid Event, 20 - 24 June 2022
In-Person: Clayton Hotel Burlington Road, Dublin, IrelandDigital Experience: One track will be live-streamed each day in BST time zone, with on-demand recording access for all other tracks made available from Monday 27th June. Learn more on the Digital Experience page.

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 in the application and development of chemical-biological methods for biomaterial characterization and biocompatibility evaluation. 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