Amendments to the Standards of in vitro diagnostic Medical Device Good Manufacturing Practices; (16 page(s), in Korean)
12 มิถุนายน 2566

แจ้งเวียนกฎระเบียบอื่น ๆ

04 พ.ย. 65

Normative Instruction 189, 26 October 2022; (1 page(s), in Portuguese)
12 มิ.ย. 68

Draft Commission Implementing Decision not approving epsilon-metofluthrin as an active substance for use in biocidal products of product-type 19 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council; (4 page(s), in English)
18 มี.ค. 68

Chief Executive's Decision No. 168/2024 (8 pages, in Chinese and Portuguese)