sr. consultant regulatory affairs
Qarad (part of QbD Group), Belgium
Pieter holds a PhD in Biotechnology with an academic career in the field of molecular immunology. Leaving academia, he joined a multinational IVD manufacturer, after which he held senior management positions in a global CRO for the laboratory component clinical trials. Pieter is currently a regulatory affairs consultant, specialized in European IVD regulations. He supports IVD manufacturers around the globe from start-up companies to multinationals, as well as laboratories and biotech companies, in their needs to comply with IVDR. Pieter is also co-chair of the Belgian RAPS LNG.
Disclosure information not submitted.
Strategies for Co-Development of Companion Diagnostics and Medicines in the IVDR Era
Wednesday, October 23, 2024
3:00 PM - 4:00 PM CEST