Medical device registration for Class C and D medical devices in Vietnam is often rejected not due to missing documents, but because of inconsistencies in product classification, intended use, and dossier structure.

为何医疗器械上市流通注册资料在资料“齐全”的情况下仍被要求补充(C类、D类)?必须避免的4个严重错误

26 3 月, 2026
Cosmetic PIF Dossier in Vietnam infographic showing the four-part structure of the Product Information File including administrative documents, raw material quality, finished product quality, and safety assessment.

越南化妆品PIF档案全面指南(2026更新版)

28 3 月, 2026