Paolo Acquafondata

I bring with me a work background of more than 25 years in which I have had the opportunity to hold
various roles as production manager, supply chain, logistics, quality control, quality assurance in various
pharmaceutical and in vitro medical device companies in Italy, Europe and worldwide.
Thanks to this experience, to my knowledge of lean management and to my knowledge of occupational
health and safety laws, I have been able to build a consultancy business in the creation of quality
systems in the pharmaceutical, medical device and in vitro diagnostic medical device sectors that take
into account regulatory requirement by integrating them with company flows, with the Lean philosophy
and with company profit aspects.
Since 2018 trainer for notified body BSI on new European regulations for medical devices and IVD
medical devices.
Since 2021 Global lead auditor for UCB Pharma.
I am also project leader of the working group at UNI (Italian Standardisation Body) for the drafting of a
reference practice on the distribution of pharmaceutical and medical products.