Liz GommansTechnical Professional at DEKRASpeaker
Profile
Liz Gommans joined DEKRA B.V. over 4 years ago, where she is the 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 in industry as a researcher in the IVD field, developing quality controls for near-patient, clinical chemistry and many other type of IVD tests.
Agenda Sessions
Chairperson’s Opening Remarks: In Vitro Diagnostic Workshop
, 09:00View SessionChairperson’s Afternoon Remarks: In Vitro Diagnostic Workshop
, 14:10View Session