Prepare, submit, track and follow through closure required initial, supplemental/interim, and final reports for Pulmonx's global product portfolio, including U.S. Medical Device Reports (MDRs), EU vigilance reports, and adverse-event reports for Japan and other OUS markets, including through authorized representatives, license holders, or in-country partners, as applicable. Support U.S. post-market reporting (PMA annual reports, 30-day notices, MDRs), labeling compliance, and license maintenance; support EU MDR post-market documentation (CERs, PMCF, PSURs, PMS plans, Technical Documentation); and conduct regulatory impact assessments for changes across U.S., EU, and global markets.