Madeline Ganton

Madeline is a Regulatory Operations Consultant and is responsible for ensuring that regulatory submissions to FDA are appropriately published according to relevant guidances and are free of technical issues.  She assists in formatting and preparing submissions for filing to the U.S. Food and Drug Administration (FDA).  Madeline has previous experience in maintaining FDA compliance and assisting in 510(k) regulatory submissions.  Madeline has a B.A. in Public Policy with a minor in Health and Environment from Michigan State University.