Senior Consultant IVD - Regulatory Affairs
Qarad
Pieter is a senior regulatory affairs IVD consultant at Qarad (part of QbD Group). Pieter holds a PhD in Biotechnology with an academic career in the field of molecular immunology and a technical expertise in flow cytometry. Leaving academia, he joined Becton Dickinson after which he held senior management positions in a global central laboratory CRO, where he was responsible for the IVDs used in clinical trials as well as for the development of clinical trial-specific tests. At Qarad, he compiled the Technical Documentation of the first Class C device certified under the IVDR and as a consultant, he supports IVD manufacturers from start-up companies to multinationals, as well as laboratories and laboratory consortia who want to comply with IVDR requirements.
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Sponsored Presentation: Transitional Provisions of the IVDR – Can I Sit Back and Relax?
Tuesday, May 7, 2024
13:00 – 13:30 CEST
CTA with Devices: State of Play for Non-CE Marked Diagnostic Tests in European Clinical Trials
Wednesday, May 8, 2024
10:25 – 11:25 CEST