Commission proposal for a Regulation of the European Parliament and of the Council amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and amending Regulation (EU) 2022/123 as regards the support of the European Medicines Agency for the expert panels on medical devices and Regulation (EU) 2024/1689 as regards the list of Union harmonisation legislation referred to in its Annex I, COM(2025)1023 final of 16.12.2025; (170 page(s), in English), (46 page(s), in English)

Regulations, No.: DFAR/HMDAR/TRG/002 Rev_2, Governing Registration of Medical Devices including In Vitro Diagnostics; (13 page(s), in English)

Draft Circular Promulgating the list of chemicals and insecticidal and disinfectant products for household and medical use which are under the state management of the Ministry of Health and whose HS codes can be indentified according to Vietnam's nomenclature of exports and imports; (9 page(s), in Vietnamese)