Alexandra Andry
Regulatory Affairs Consultant @Alispharm
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WORK HISTORY
Regulatory Affairs Consultant @Alispharm
FR
Medical Device Regulation compliance activities ( update of Design History File, notified body submission.)- Gap assessment on Medical Device Regulation parts ( template, procedures )- Update of technical files for registration during devices life cycle - Develop and maintain Regulatory Affairs process and activities - Regulatory watch : analyze and communicate worldwide regulatory requirements and regulations for medical devices
EDUCATION
University of Montpellier
Health Engineering, Conception and production of health products
Technological University Dublin
Bachelor of Science - BS, Science/ Bioanalysis/ Operations and Quality Management
ABOUT ALEXANDRA ANDRY
Regulatory Affairs Consultant at AlisPharm
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