RA specialist/Technical specialist
DEKRA B.V.
Arnhem, Gelderland, Netherlands
Liz Gommans joined DEKRA B.V. over 5 years ago, where she is a regulatory affairs specialist mainly focusing on IVDR and a member of several Team NB focus groups. In addition, she is a qualified technical file reviewer for IVDD and IVDR.
Prior to joining DEKRA, Liz studied molecular life sciences in the Netherlands. She obtained her PhD in the field of glycobiology, performing research on the interface between chemistry and biology. After her PhD, she worked several years in industry as a researcher in the IVD field, developing quality controls for near-patient, clinical chemistry and many other type of IVD tests.
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Mastering Post-market Surveillance Under IVDR: From PMPF to PSUR
Friday, May 16, 2025
10:30 - 11:30 CEST