On July 30, 2025, the Medical Device Authority (MDA) released an official announcement regarding the Implementation of the Malaysia–China Medical Device Regulatory Reliance Programme (Pilot Phase I). The programme is a result of a Memorandum of Understanding (MoU) signed between the MDA (Malaysia) and the National Medical Products Administration (NMPA)
On July 22, 2025, the Head of the National Public Procurement Agency (Lembaga Kebijakan Pengadaan Barang/Jasa Pemerintah – LKPP) issued Circular Letter No. 2 of 2025 concerning the Deactivation of the e-Catalogue Version 5 for Construction and Health Showcases. To view the official document (Bahasa Indonesia only), refer to:Circular Letter
On July 23, 2025, the Thai Food and Drug Administration (Thai FDA) announced a new system for the renewal of medical device licenses and notification certificates, to be submitted annually through the SKYNET online platform. To view the official announcement and infographic, refer to:กองควบคุมเครื่องมือแพทย์ (Medical Device Control Division) Key Highlights
On July 18, 2025, the Thai Food and Drug Administration (FDA) issued a press release clarifying the differences between the Document Addition System (Upgrade to Full CSDT) and the Renewal System within SkyNet, the regulatory platform for medical device registrations. This clarification is critical for stakeholders managing existing licenses or
On July 18, 2025, the Ministry of Public Health, acting on the recommendation of the Medical Device Committee, issued an announcement revising the official list of designated inspection points for imported medical devices. This update repeals and replaces the previous Announcement dated December 14, 2023 (B.E. 2566). To view the
On July 21, 2025, the Vietnam Ministry of Health issued Official Dispatch No. 4755/BYT-HTTB to solicit public and stakeholder feedback on the Draft Circular concerning the issuance of a national centralized procurement list for medical devices and testing supplies. This draft, prepared by the Infrastructure and Medical Device Administration (IMDA),
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