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Daniele Bollati
Product Conformity Assessment /Medical Devices Expert at IMQ

Profile

DANIELE BOLLATI: 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

  • Creating a Robust QMS System that can Successfully Process the EU MDR

    11:05
  • NOTIFIED BODY FEEDBACK: Post Market Surveillance - How to Succeed in the First Year Under EU MDR

    10:35
  • NOTIFIED BODY PANEL DISCUSSION: EU MDR Pain Points

    13:55