I have extensive medical device regulation experience, including marketing, warning concerns, and device post-approval processes. I have experience in RA/Clinical and RA/QA at various levels including specialist, director, client manager, project manager, third party, expert witness, and consultant. I previously served as the lead regulator on device and combination product submissions and clinical trial submissions to FDA. I have received 54 FDA approvals for medical devices in the past 9 years, and have received FDA approval for 6 clinical trials in that same period. I have submitted and managed 24 presubmission packages to FDA and held hundreds of meetings and conference calls with the FDA during that time. I have managed experts and testing labs globally to complete product testing and respond to AI requests on time. I have also managed human factor and usability studies, biocompatibility studies, sterilization and disinfection validations, packaging validations, shelf life and life of device programs, electrical and EMC safety testing, software validations, performance testing, risk assessments, conditioning and cleaning validations for reprocessed equipment, and radiation safety reporting as part of applications and AI responses. I have managed and developed promotional and advertising campaigns and evaluated the post-approval off-label marketing, including adulteration and misbranding. I have advised on corporate quality and regulatory compliance issues. To ensure compliance with regulatory requirements and QMS regarding supplier controls, manufacturing, sterilization, promotion and labeling, complaint handling, CAPA, and PMS requirements, I have implemented investigations into complaints, adverse events, recalls, and non-conforming material reviews. I have experience drafting expert reports on regulatory and quality topics for medical devices and combination products.