Wendy Decker is a Sr. International Regulatory Affairs Specialist at Werfen, where they prepare regulatory submissions and manage interactions with the FDA and international regulatory bodies. With experience in various regulatory roles, including positions at The Marena Group and CryoLife, they have developed expertise in generating Standard Operating Procedures and maintaining compliance with federal and international regulations. Wendy is pursuing a degree in Health Information Technology at DeVry University, having previously completed studies in Health Information Technical Management.
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