Annick Barthod-Malat has extensive experience in regulatory affairs and quality management in the biomedical field. Annick worked as an Intervenante Affaires Réglementaires at ISIFC from October 2013 to November 2016, where training was provided on the 60601 standard related to electromedical devices. From September 2011 to July 2017, Annick served as Responsable Qualité Affaires Réglementaires at Maincare, focusing on European market submissions, CE marking documentation for electromedical systems, and implementing ISO 13485 quality management systems. Subsequently, from January 2018 to March 2023, Annick held the position of Responsable Qualité & Affaires Réglementaires at Biosency, with responsibilities including product modifications analysis and post-market surveillance. Currently, since October 2022, Annick is a Chef de projet at Biosency. Annick holds a Diplôme d'ingénieur in Génie biomédical from the Institut Supérieur d'Ingénieurs de Franche-Comté, completed in 2011.
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