Views:13 Author:Site Editor Publish Time: 2019-09-21 Origin:Site
Name：InterTabac 2019
Time：Sept. 20-22, 2019
Address：Dortmund, Germany
A new rule from the Drug Enforcement Administration (DEA) threatens to upend the American hemp industry, and could even result in criminal prosecutions for manufacturers of CBD and delta-8 THC products.The DEA says the “interim final rule,” issued Aug. 20, is simply a matter of adjusting its own reg
The Family Smoking Prevention & Tobacco Control Act requires that all tobacco products must receive a PreMarket Tobacco Application (PMTA) authorization before they can be sold across the U.S..Initially set for May 12th, as the deadline was approaching, a number of entities including Altria Group In
In August 2020, YOUME subsidiary vape brand Suorin has submitted a PMTA application to FDA.What is PMTAPMTA is abbreviation for “Premarket Tobacco Product Applications for Electronic Nicotine Delivery System”, which initiated by FDA on June of 2019. Essentially a PMTA involves compiling and submitti
A group of small vaping manufacturers and trade organizations has requested that the FDA ask a federal court for permission to postpone the Sept. 9 PMTA deadline for 180 days. The companies say they have been prevented from complying with the process by the coronavirus pandemic. Now they have just t
Name：TPE 2020Time：Jan. 29-31, 2020Address：Las Vegas, US
DO NOT USE THIS PRODUCT IN THE FOLLOWING SITUATIONS:
• Are under the legal age of purchase
• Are pregnant or breastfeeding
• Have heart disease, stomach or duodenal ulcers, liver or kidney problems, throat disease, or difficulty breathing due to bronchitis, emphysema, or asthma
• Have an overactive thyroid or pheochromocytoma a tumor of the adrenal gland that can affect blood pressure)
• Are taking certain medications, such as theophylline, ropinirole, or clozapine .
