Clémence Pupier

Clémence Pupier has a diverse work experience in the field of Quality and Regulatory Affairs. Clémence began their career in 2016 as a Stage Matériovigilance at CHU de Saint-Etienne, where they were responsible for writing activity reports, monitoring material vigilance cases, and participating in multidisciplinary meetings.

In 2016, they also worked as a Regulatory Affairs Assistant at SERF - Société d'Etude, de Recherche et de Fabrication. Clémence'smain responsibilities included updating technical documentation, preparing CE marking files for medical devices, and conducting chemical characterization tests in compliance with ISO standards.

Since 2017, Clémence has been employed at Cardiawave. Clémence initially joined as a Quality and Regulatory Affairs Project Manager and later transitioned to the role of Quality & Regulatory Affairs Manager. Details about their specific responsibilities during these roles are not provided.

Clémence Pupier's education history began in 2011 at Université Jean Monnet Saint-Etienne, where they pursued a PACES program in the field of study. From 2013 to 2015, they attended Université Claude Bernard Lyon 1 and obtained a Bachelor's degree in Biochemistry. Following that, between 2015 and 2016, Clémence pursued a Master's degree in Engineering for Health and Drug from the Institut de Pharmacie Industrielle de Lyon (IPIL). Finally, in 2016 and 2017, they attended Polytech Lyon, where they completed a Master's degree in Regulatory Affairs for medical devices.