Lead for European Regulation
Central Committee on Human Research
After an extensive career as pharmaceutical and medical device regulator in the Dutch government, serving subsequently in the Medicines Evaluation Board and Ministry of Health, she joined Philips in 2011 as Lead for European Regulation. She acted as leader and expert in European Medical Device and Pharmaceutical Regulations and Standards on corporate level and was involved as Subject Matter Expert in Philips’ EU MDR/IVDR Implementation Program. She was Vice-Chair of the EU Regulatory Affairs Focus Group and Chair of the Clinical Working Group in COCIR and Member of Regulatory Affairs Committee in MedTech Europe.
In 2018 she returned to civil service by accepting the position of scientific staff member medical devices at CCMO, the governmental organization for clinical investigations in the Netherlands. At CCMO she was tasked with the implementation of the EU MDR/IVDR and she was representing the Dutch competent authorities in the CIE (Clinical Investigation and Evaluation WG of EU Commission). In 2019 she transferred to the Ministry of Health.
Sabina has a long track record as volunteer in global professional organizations (DIA and RAPS) and is a regular speaker and faculty member in educational conferences on regulatory topics. For her contributions to the regulatory profession she has been awarded as Fellow of RAPS in 2015.
Saturday, September 21
9:00 AM – 5:00 PM