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Global Pharmaceutical Regulatory Affairs Summit


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22-24 October 2024
Sheraton Brussels Airport, BrusselsHybrid Event

Josef Pellizarri
Managing Director at Pellizzari Consulting GmbH


Dr. Josef Pellizzari has more than 20 years of experience in the pharmaceutical industry, focusing on structured authoring and the data flow towards Regulatory Affairs. He was consequently part of the PIM, XEVMPD and IDMP initiatives of major pharmaceutical companies. Dr. Pellizzari started his career on the IT side and has been at the interface of RA and IT for approximately a decade, resulting in the double competency to be able to apply data science techniques to RA data while being intimately familiar with the RA processes and ways of working.

Since 2021 Dr. Pellizzari works as an independent consultant specialized in IDMP and RIM systems. He also contributes to the ISO IDMP standards as well as the EMA Implementation Guide.

Agenda Sessions

  • Analysing your migrated data in PMS