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  • Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 (COM(2023)193 final); (182 page(s), in English), (37 page(s)
Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 (COM(2023)193 final); (182 page(s), in English), (37 page(s)
14 กันยายน 2566

แจ้งเวียนกฎระเบียบอื่น ๆ

17 ก.ค. 67

Establishment of the labelling information with respect to measures, etc., for preventing environmental pollution attributable to the relevant class II specified chemical substances, to be indicated on containers, packaging, or invoices for NPE or the products specified in Article 9 of the Order for Enforcement of the Act on the Regulation of Manufacture and Evaluation of Chemical Substances which use NPE; (2 page(s), in English)
27 ก.ย. 66

Draft Commission Delegated Regulation supplementing Directive (EU) 2020/2184 of the European Parliament and of the Council by establishing harmonised specifications for the marking of products that come into contact with water intended for human consumption; (5 page(s), in English), (2 page(s), in English)
10 ก.พ. 66

"Addendum to Administrative Order No. 50 s.2001 entitled "Revised 2001 Schedule of Fees and Charges for the Corresponding Services Rendered by the Bureau of Food and Drugs"; (3 page(s), in English)