With over 15 years regulatory experience in medical devices, Rozanne has in-depth experience working on US and International pre- and post- market regulatory activities, FDA inspections, Notified Body audits and many complex projects including manufacturing site changes, legal manufacturer changes, Notified Body transfers, acquisitions, integrations and divestitures. Rozanne has a passion for acquisition and integrations and appreciates the challenges it brings. She enjoys working to minimize impact to the business during transitions.