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Global Pharmaceutical Regulatory Affairs Summit
22-24 October 2024
Sheraton Brussels Airport, BrusselsHybrid Event

Veronica Lipucci Di Paola
Master Data Manager at European Medicines Agency at EMA
Speaker

Profile

Veronica Lipucci Di Paola joined the EMA in 2014, where she has worked ever since covering various roles. She holds a Master in Regulatory Affairs from TOPRA & University of Hertfordshire, a pharmacy degree and more than 10 years of data management experience in the field of Medicines for human use (area of pharmacovigilance and regulatory affairs). As PMS Co-Product Owner she is responsible to deliver, coordinate and maintain the Product Management Services (PMS) as well as implementing ISO IDMP standards in Europe. Veronica works closely with the business and technical colleagues, the development teams as well as Industry and Network stakeholders’ groups.

She is a nominated EDQM Standard Terms Working Party’s expert and ISO IDMP member. Prior joining the Agency, she worked as pharmaceutical consultant and in the regional pharmacovigilance hospital center.

Agenda Sessions

  • Electronic Application Forms (eAF): Where does Web eAF fit in with intended Target Operating Model?

    09:55