Ferrosan Medical Devices
Joan Drejer is a seasoned regulatory affairs professional with extensive experience in the medical devices sector. Currently serving as Director RA at Ferrosan Medical Devices A/S since April 2021, Joan previously held senior roles including Director of Global RA Operations & Biosafety at Coloplast and Chief Officer RA & QA at Nanovi A/S. Joan's expertise encompasses strategic regulatory direction for medical devices across various classifications, ensuring compliance with global legislation, including European and FDA requirements. With a strong foundation in regulatory strategies developed during tenure at Santaris Pharma, Joan holds a PhD from Danmarks Farmaceutiske Universitet.
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