Statute-Shenzhen DTi Technology Testing Co., Ltd.

19

2024.07

FDA Authorizes Marketing of Vuse Alto Tobacco-Flavored E-Cigarette Pods and Acco

the U.S. Food and Drug Administration (FDA) authorized the marketing of seven e-cigarette products in the United States through the premarket tobacco product application (PMTA) pathway.
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17

2024.07

FDA and DOJ Action Leads to Permanent Injunction Against E-Cigarette Manufacture

The court also ordered Soul Vapor and Mr. Jeffrey to destroy e-cigarette products that were manufactured by Soul Vapor and are in their custody, control, or possession.
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14

2024.06

FDA warns of sales of unauthorized e-liquids that resemble prescription pill bot

On June 13, the FDA announced that it had issued warning letters to six online retailers for selling unauthorized e-cigarette oil products from the Bad Drip brand that imitated prescription medication bottles.
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09

2024.05

Restriction proposal on chromium (VI) to cover more substances

The European Commission has requested ECHA to broaden the scope of the REACH restriction proposal to cover at least 12 chromium (VI) substances.
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08

2024.05

FDA, DOJ Seize Over $700,000 Worth of Unauthorized E-Cigarettes

Today, the U.S. Food and Drug Administration (FDA), in coordination with the U.S. Department of Justice (DOJ), announced that the U.S.
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06

2024.05

FDA Issues Warning Letters to 14 Online Retailers for Selling Unauthorized E-Cig

On May 1, FDA announced the issuance of warning letters to 14 online retailers for selling unauthorized e-cigarette products popular among youth.
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24

2024.04

FDA Seeks Approximately $20,000 Each from 22 Retailers Selling Elf Bar and Other

On Apr. 23. FDA announced the issuance of complaints for civil money penalties (CMPs) against 20 brick and mortar retailers and two online retailers for the sale of unauthorized e-cigarettes, including Elf Bar, a popular youth-appealing brand.
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16

2024.04

FDA Denies Marketing for 65 “MNGO Disposable Stick” E-Cigarettes

On April 15, the FDA issued a marketing denial order (MDO) to Shenzhen Yibo Technology Co., Ltd. for 65 disposable e-cigarettes named "MNGO Disposable Stick".
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11

2024.04

Introduction to U.S. Tobacco Product Premarket Application (PMTA)

In order for new tobacco products to be sold legally in the United States after February 15, 2007, they must submit an application to the U.S. Food and Drug Administration, review and obtain approval.
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09

2024.04

New CLP hazard classes will be included in IUCLID

Companies can soon start including information on new hazard classes in their IUCLID dossiers, following the amendment of the Classification, Labelling and Packaging (CLP) Regulation.
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FDA Authorizes Marketing of Vuse Alto Tobacco-Flavored E-Cigarette Pods and Acco

FDA and DOJ Action Leads to Permanent Injunction Against E-Cigarette Manufacture

FDA warns of sales of unauthorized e-liquids that resemble prescription pill bot

Restriction proposal on chromium (VI) to cover more substances

FDA, DOJ Seize Over $700,000 Worth of Unauthorized E-Cigarettes

FDA Issues Warning Letters to 14 Online Retailers for Selling Unauthorized E-Cig

FDA Seeks Approximately $20,000 Each from 22 Retailers Selling Elf Bar and Other

FDA Denies Marketing for 65 “MNGO Disposable Stick” E-Cigarettes

Introduction to U.S. Tobacco Product Premarket Application (PMTA)

New CLP hazard classes will be included in IUCLID

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