Как проверить статус ЭПТС по VIN на portal.elpts.ru перед покупкой авто. Разница между публичным поиском и выпиской собственника, защита данных по 152-ФЗ, пошаговый чек-лист.
Verify FDA establishment registration and device listing with this 4-step CDRH database audit workflow for medical device exporters and buyers.
2026年第21号公告规定2027年6月1日起全部二类器械及一类IVD须具备UDI并完成数据库上传；已纳入医保代码数据库的产品须完成医保代码对接。本文深度解读合规要求与四大误区。
FDA foreign drug establishment registration: timing, site DUNS, U.S. agent and importers, annual renewal, SPL filing and approval boundaries.
FDA labeler code checklist covering DUNS, SPL submission routes, the 30-day update scope, and conditional two-year deactivation.
FXR0906 clinical trial China: what Fosun reported about NMPA clinical-trial approval, what remains unknown about Phase 1, and evidence boundaries.
What FDA Global Generic Drug Affairs does and does not do: Generic Drug Cluster, PSA pilot, and ANDA submission boundaries for overseas teams.
FDA drug registration and listing compliance map: current SPL, EDRLS, and 510(j)(3) duties, plus the future 12-digit NDC timeline.
GDUFA III decision map for generic drug developers: controlled vs general correspondence, pre-ANDA meetings, post-CRL, PSG, and CPA boundaries.
