Karen Tsuyama is a dedicated regulatory affairs professional with extensive experience in the medical device and clinical research sectors. Currently serving as a Regulatory Affairs Manager at Fiagon since July 2022, Karen previously held roles as a Senior Regulatory Affairs Specialist at Teleflex Latin America and Medtronic, where responsibilities included leading teams, developing standard operating procedures, and managing regulatory submissions with ANVISA. Karen's career also encompasses clinical research expertise, having worked as a Clinical Research Specialist and Clinical Research Associate with PPD, ensuring compliance with GCPs and regulatory standards. Karen's educational background includes a degree from Universidade Santo Amaro, completed in 2010.
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