I hold a Master’s degree in product and process engineering, specialising in production management and organization. My career first began in the cosmetics sector and, strangely enough, in regulatory affairs! Now I’ve been happily working in regulatory affairs for nearly ten years ! I joined the nexialist adventure in 2014, where I discovered the dynamic world of medical devices. The good news: the medical device sector is taking the same regulatory turns as the cosmetic sector.
My mission is to support manufacturers in placing on the market medical devices that comply with the applicable regulations in force. I work at a very early stage of the product life cycle, in particular by carrying out strategic regulatory studies. In 2018, I became Director of our Knowledge Management Department. My team and I dissect and analyse regulations and standards related to MD and IVD and all information affiliated with these sectors. We make these texts understandable through different means of communication for both our consultants and clients. At nexialist, the understanding and transfer of information and knowledge is at the heart of our job. Our work is certainly cut out for us!