Daniele Lioi is a Senior Consultant and Business Unit Manager of the Eurofins Italian Medical device consultancy team
Since 2017, he has been dealing with Biological Risk assessments, Clinical Evaluation and Supporting the compilation of the technical documentation for medical device manufacturers. He has a biotechnology background with experience in regulatory affairs of medical devices. Daniele obtained the qualification as Auditor/Lead Auditor ISO 13485/ISO 9001, he is included in the national registry for person responsible for regulatory compliance and he joined the HAS consultants team for the harmonization of International Standards.