Medical writer director
More than 14 years of medical writing expertise at Namsa. Since 2012, authored and co-authored more than 130 clinical evaluation reports (CERs) for all class medical devices (class I, IIa/IIb and III) according to the MEDDEV 2.7.1 Rev. 3 (2009) and MEDDEV 2.7/1 Rev. 4 (2016), MDD, EU Medical Device Regulation (MDR) 2017/745 and In-Vitro Medical Device Regulation (IVDR) 2017/746.
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