Duccio Lombardi graduated in Medical and Pharmaceutical Biotechnologies, after the Pharmacology and Innovative Therapies Ph.D., he focused on the Quality area of the Pharmaceutical Companies field.
Having a broad knowledge of FDA, EMA, MHRA, and other regulations, his first focus was on Data Integrity; later on, he decided to step into Serialization and Track and Trace as EU FMD Serialization Quality Unit Responsible in his Company where he was mostly focused on Alert Management, competent Authority interface and innovations aimed to enhance Quality within the everyday fight against counterfeiting as well as to decrease effort in managing FMD False (positive) Alerts.
He then stepped into the role of Serialization Normative Compliance and Anti-Counterfeiting Corporate Quality Unit Head focalizing on worldwide Regulative Framework application and Compliance adherence for the Company, as well as having a special focus on innovation and intervention strategies to tackle operative and qualitative issues to worldwide normative conformity.
EVENTS & ACTIVITIES (Speaking, Spoken, and Authored)