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2026.08
Today, the U.S. Food and Drug Administration (FDA), authorized the marketing of 11 new nicotine pouch products through the premarket tobacco product application (PMTA) pathway.
10
On August 4, the U.S. Food and Drug Administration (FDA) approved four new nicotine pouch products for market through the Premarket Tobacco Product Application (PMTA) pathway.
01
2026.07
Today, the U.S. Food and Drug Administration (FDA) issued modified risk granted orders to Swedish Match USA, Inc. for 20 ZYN nicotine pouch products following extensive scientific review.
20
2026.05
Faced with increasingly stringent market access rules from the EU and the high pressure of routine overseas inspections, Shenzhen Dezewei, with 16 years of testing and certification experience, has developed a systematic compliance solution for electronic
12
FDA is committed to combating illicit tobacco products in this country.
09
On April 30, 2026, Argentina passed Resolution No. 549/226 of the Ministry of Health and its annex "Requirements for Registration, Sale, and Inspection of Tobacco and Nicotine Products".
07
The U.S. Food and Drug Administration (FDA) today authorized the marketing of four Glas electronic nicotine delivery systems (ENDS) through the premarket tobacco product application (PMTA) pathway.
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2026.04
On April 22nd, the US Food and Drug Administration (FDA) released the Federal Register, officially adding 18 ingredients to the list of harmful and potentially harmful substances (HPHC) in tobacco products.
22
2026年4月20日,欧盟官方公报正式发布REACH法规((EC) No 1907/2006)修订条例(EU) 2026/859。
03
The European Commission has released implementation guidelines for the Packaging and Packaging Waste Regulation (PPWR), aimed at promoting the uniform implementation of new packaging rules within the EU.
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