ส่งเสริมการส่งออกผลิตภัณฑ์สุขภาพส่งเสริมการส่งออกผลิตภัณฑ์สุขภาพhttps://export.fda.moph.go.thth1110810Draft of Egyptian standard ES 1595-3 for " Single-use medical examination gloves Part 3: Specification for gloves made from poly (vinyl chloride) ".; (15 page(s), in English)https://export.fda.moph.go.th/tbt-notification/egy597/Fri, 10 Jul 26 15:09:00 +0700National Standard of the P.R.C., Medical electrical equipment — Part 2-85: Particular requirements for the basic safety and essential performance of cerebral tissue oximeter equipment; (68 page(s), in Chinese)https://export.fda.moph.go.th/tbt-notification/chn2289/Fri, 10 Jul 26 15:05:00 +0700National Standard of the P.R.C., General requirements on raw materials of toothpastes; (248 page(s), in Chinese)https://export.fda.moph.go.th/tbt-notification/chn2270/Fri, 10 Jul 26 14:58:00 +0700Draft Order of the Ministry of Health of Ukraine "On Approval of the Procedure for Imposing a Prohibition (Temporary Prohibition) and Withdrawal of Medicines from Circulation on the Territory of Ukraine"; (24 page(s), in Ukrainian)https://export.fda.moph.go.th/tbt-notification/ukr396/Thu, 09 Jul 26 14:54:00 +0700Draft Order of the Ministry of Health of Ukraine "On Approval of Amendments to the Procedure for the Notification (Submission) of Information on Cosmetic Products"; (3 page(s), in Ukrainian)https://export.fda.moph.go.th/tbt-notification/ukr395/Wed, 08 Jul 26 14:44:00 +0700Draft Commission Implementing Decision on the non-approval of 1,3- Bis(hydroxymethyl)-5,5-dimethylimidazolidine-2,4-dione (DMDMH) as an existing active substance for use in biocidal products of product types 6 and 13in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council; (4 page(s), in English)https://export.fda.moph.go.th/tbt-notification/eu1222/Wed, 08 Jul 26 14:37:00 +0700Draft Commission Implementing Decision (EU) repealing Implementing Decision (EU) 2026/1089 postponing the expiry date of the approval of medetomidine for use in biocidal products of product-type 21 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council; (3 page(s), in English)https://export.fda.moph.go.th/tbt-notification/ำี/Wed, 08 Jul 26 14:33:00 +0700Draft Commission Implementing Decision (EU) not renewing the approval of medetomidine as an active substance for use in biocidal products of product-type 21 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council; (6 page(s), in English)https://export.fda.moph.go.th/tbt-notification/eu1220/Wed, 08 Jul 26 14:29:00 +0700Amending Regulation (EC) No 1223/2009 of the European Parliament and of the Council as regards the use in cosmetic products of certain substances, including those classified as carcinogenic, mutagenic or toxic for reproduction.; (18 page(s), in English)https://export.fda.moph.go.th/tbt-notification/eu1219/Wed, 08 Jul 26 14:23:00 +0700Draft Resolution of the Cabinet of Ministers of Ukraine "On Amendments to Resolution of the Cabinet of Ministers of Ukraine No. 65 of 20 January 2021" (concerning Technical Regulation on cosmetic products); (2 page(s), in Ukrainian)https://export.fda.moph.go.th/tbt-notification/ukr392/Fri, 03 Jul 26 14:45:00 +0700