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Giorgio Angelo Molteni is a Regulatory Affairs Lead and Safety Officer at Roche Diagnostics Italy since January 2024, previously serving as Regulatory Affairs & Quality Manager at the same company. With a career at Roche Diagnostics starting in 1994, Giorgio has extensive experience in medical device vigilance, managing customer complaints, and maintaining medical device repertory. Additionally, Giorgio is certified as a Quality Auditor and is responsible for recording safety data into the Istituto Superiore Sanità website. Prior to this, Giorgio worked as a Product Specialist at Bio-Rad Laboratories from 1991 to 1993. Giorgio holds a degree in Chemistry and Pharmaceutical Technology from Università degli Studi di Milano.