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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.
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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
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FDA is committed to combating illicit tobacco products in this country.
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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".
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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.
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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。
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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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2026.03
ECHA's two scientific committees support EU-wide action with appropriate derogations and controls to address the growing and long‑lasting risks per-and polyfluoroalkyl substances (PFAS) pose to people and the environment.
On March 11, 2026, the UK Health and Safety Executive (HSE), the regulatory body for REACH, announced the launch of a 6-week public consultation to solicit opinions on the inclusion of 15 substances of high concern (SVHC) in the UK REACH candidate list.
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