Mariëtte Schrier has been working as MDR advisor within Hogeschool Utrecht at the Smart Systems for Healthy Living lectorate since mid-March 2025. In addition to years of experience in research as a molecular biologist, she has extensive experience in clinical trials and the Medical Device Regulation (MDR).
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Mariëtte believes that innovation in healthcare is important and enjoys helping to make medical device regulations more accessible, ensuring that more innovative projects successfully reach the market.
Fields of expertise
- Medical Device Regulation
- Clinical Trials
- ISO 13485