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Aimée Ramos has a wealth of experience in the medical device industry. Aimée began their career in 2011 as a Stagiaire in a research laboratory for genetic and pathophysiology of mental retardation at INSERM. In 2014, they joined Moria SA as a Regulatory Affairs Officer, where they created and updated technical files for CE marking according to directive 93/42 / EEC. Aimée also acted as a liaison between internal departments, notified bodies and ANSM and implemented the medical device regulation 2017/745. Later in 2014, Aimée was promoted to Quality and Regulatory Affairs Officer at Moria SA, where they managed international device registrations. In 2021, Aimée joined Peters Surgical as an International Regulatory Affairs Manager.

Aimée Ramos completed a Master 1 in Biochimie et biologie cellulaire from CY Cergy Paris Universit\u00e9 in 2012-2013, followed by a Master 2 professionnel in Biochimie des mat\u00e9riaux et du vivant from CY Cergy Paris Universit\u00e9 in 2013-2014.