Regulatory Strategy Principal
TUV SUD Product Service GmbH
Sabina has 20 years of experience as pharmaceutical and medical device regulator in the Dutch government, serving subsequently in the Medicines Evaluation Board, Ministry of Health and the governmental organization for clinical investigations CCMO.
She has worked in global medtech industry as Lead for European Regulation in Philips, where she acted as leader and expert in European Medical Device and Pharmaceutical Regulations on corporate level and was involved in Philips’ EU MDR/IVDR Implementation Program.
Currently, she is Regulatory Strategy Principal at TÜV SÜD and acting as representative of TÜV SÜD and Notified Bodies in regulatory working groups at European level. She is Chair of NB-MED, the formal EU Commission’s working group of Notified Bodies and Vice-President of Team-NB, the EU Notified Bodies’ association.
Sabina has a long track record as volunteer in global professional organizations (DIA and RAPS). She is a regular speaker and faculty member in educational conferences on regulatory topics.
She was co-founder and Chair of the RAPS Netherlands Chapter. She is Fellow of RAPS since 2015 and serves in the RAPS Global Board of Directors since 2020.
Monday, September 14, 2020
10:00 AM – 11:30 AM EDT