Petition Against E-cigarette Ban Gains 50k Signatures in Kazakhstan

2Firsts Events by Alice Wang
Jun.15.2023
Petition Against E-cigarette Ban Gains 50k Signatures in Kazakhstan
A petition with 50,000 signatures is challenging e-cigarette ban in Kazakhstan due to poor enforcement of existing laws.

A petition opposing the ban on e-cigarettes has reached 50,000 signatures in Kazakhstan, according to Orda. Under the country's laws, petitions with at least 50,000 supporters must be considered by the government. The petition has been submitted to the National Assembly. Its organizer, Tatiana Fominova, is calling on citizens to reconsider the ban, as the country's lower house of parliament discusses the feasibility of banning e-cigarettes.

 

Background and Issues of the Ban Discussion

 

The debate surrounding a ban on e-cigarettes in Kazakhstan continues to escalate, primarily due to concerns about the sale of these products to minors. While Kazakhstani law already prohibits the sale of e-cigarettes to those under 18 years old, this legislation has done little to prevent the market from selling these products to teenagers.

 

At present, e-cigarettes have not yet been certified, and there are no legal provisions regarding the prohibition of placement and public display.

 

Anton Shishkovsky, the Chairman of the Kazakhstan E-Cigarette Association, stressed that the issue of selling e-cigarettes to minors is due to a lack of regulatory measures among sellers.

 

He stated:

 

“Currently, 70% to 80% of Kazakhstan's e-cigarette market operates in a regulatory grey area due to a lack of oversight and inspection, which has been halted for three years. In the past three years, e-cigarette sales have seen significant growth.”

 

Additionally, Dmitry Zhukov, the Chairman of Qazspirits Association in Kazakhstan, expressed his dissatisfaction with the stance of the Health Ministry and the Anti-Smoking Alliance.

 

He explained.

 

“We have reported to the Ministry of Health and the Anti-Smoking Alliance about the violation of e-cigarette sales rules. However, during this period, while the rules were being violated and ignored, the Ministry of Health and the Anti-Smoking Alliance did not provide any supervision to the responsible regulatory authorities.”

 

Existing Regulations and Calls for Improvement

 

Supporters of the petition pointed out that Kazakhstan already has laws in place to prevent the sale of e-cigarettes to minors. The popularity of e-cigarettes among youth is mainly due to the ineffective enforcement of existing regulations and a lack of oversight in market monitoring.

 

Furthermore, Article 110 of the Health and Medical Code of Kazakhstan prohibits the sale of e-cigarettes to minors.

 

Similarly, tobacco products including e-cigarettes are not allowed to be sold or publicly displayed at the checkout counter.

 

Reference:

 

Kazakhstanis voted against the ban on vapes - a petition has gathered over 50,000 signatures.


Disclaimer

This article is provided solely for professional research, industry discussion, and informational purposes. Any references to brands, companies, products, technologies, or policies are made for factual reporting and analytical purposes only, and do not constitute endorsement, recommendation, promotion, or advertising by 2Firsts.

Nicotine-containing products, including but not limited to cigarettes, e-cigarettes, heated tobacco products, and nicotine pouches, carry significant health risks. Readers are responsible for complying with all applicable laws and regulations in their respective jurisdictions, including age restrictions and access limitations.

The information contained in this article should not be regarded as investment, legal, medical, regulatory, or commercial advice. While 2Firsts strives to ensure the accuracy and reliability of its content, it does not assume liability for any direct or indirect loss arising from errors, omissions, inaccuracies, or reliance on the information contained herein.

This article is not intended for individuals below the legal age for accessing tobacco or nicotine-related information in their jurisdiction.

 

Copyright Notice

This article is either original content produced by 2Firsts or content reproduced, translated, summarized, or adapted from third-party sources with attribution where applicable. The intellectual property rights of the original content remain with 2Firsts or the respective original rights holders.

No individual or organization may copy, reproduce, distribute, republish, modify, translate, or otherwise use this content without prior authorization. Any unauthorized use may result in legal action.

For copyright-related inquiries, corrections, or removal requests, please contact: info@2firsts.com.

 

AI-Assisted Translation and Editing Notice

Portions of this article may have been translated, edited, or reviewed with the assistance of artificial intelligence tools to improve efficiency and readability. Due to the limitations of AI-assisted translation and editing, discrepancies, omissions, or inaccuracies may exist when compared with the original source.

Where applicable, readers are advised to refer to the original source for the most complete and accurate information. If you identify any errors or believe that any content infringes upon your rights, please contact us at info@2firsts.com, and we will review and address the matter promptly.

Charlie’s Says 30 PACHA Vape SKUs Tentatively Identified for FDA’s Non-Priority Enforcement Public List
Charlie’s Says 30 PACHA Vape SKUs Tentatively Identified for FDA’s Non-Priority Enforcement Public List
Charlie’s Holdings said the U.S. Food and Drug Administration notified the company on June 23, 2026, that 30 PACHA vape SKUs with submitted PMTAs had been tentatively identified for inclusion on a planned public-facing FDA webpage. Under enforcement guidance issued by FDA in May, the webpage is intended to identify certain unauthorized products for which the agency generally does not intend to prioritize enforcement of premarket authorization requirements. Charlie’s disclosed the development alongside second-quarter revenue of $3.8 million, up 116% year over year.
Aug.25
UK-Listed Consumer Goods Group Supreme Sees Vape Duty as Potential Consolidation Opportunity, Holds FY27 Outlook
UK-Listed Consumer Goods Group Supreme Sees Vape Duty as Potential Consolidation Opportunity, Holds FY27 Outlook
UK-listed consumer goods group Supreme plc says it continues to expect FY27 trading to meet market expectations as the Vaping Products Duty takes effect on October 1, while maintaining a comparatively positive view of the new tax and compliance regime. Supreme has said the framework could increase compliance complexity for smaller operators and contribute to market consolidation, while its manufacturing, compliance and distribution scale may allow it to gain share. Its 88Vape brand will retain its value positioning.
Sep.18
Product | HQD SiSA 80K Enters the U.S. Market With a Hookah-Inspired Approach to the High-Capacity Disposable Segment
Product | HQD SiSA 80K Enters the U.S. Market With a Hookah-Inspired Approach to the High-Capacity Disposable Segment
The HQD SiSA 80K Hookah Disposable Vape has appeared across U.S. and cross-border online retail channels. The device comes prefilled with 28ml of e-liquid, uses a 5% nicotine salt configuration and carries a brand claim of up to 80,000 puffs. Beyond puff count, the product differentiates itself through hookah-inspired features including adjustable airflow, a flowing-water sound effect and flavor options associated with traditional hookah consumption.
Aug.18
Former Roche Neuroscience and Rare Diseases Communications Director Ria Kioupritzi Joins PMI as Scientific Affairs Director
Former Roche Neuroscience and Rare Diseases Communications Director Ria Kioupritzi Joins PMI as Scientific Affairs Director
Eleftheria (Ria) Kioupritzi, a biopharmaceutical professional with more than 15 years of experience, has joined Philip Morris International as Director Scientific Affairs within Corporate Affairs. She previously served at Roche as Senior Scientific Communications Director for Neuroscience and Rare Diseases and worked extensively in spinal muscular atrophy. Her earlier career also covered competitive intelligence, clinical and regulatory monitoring, pipeline development and launch preparation. During her time working in Roche's SMA field, Evrysdi passed through several U.S. FDA milestones, including its initial approval, an expanded indication for younger infants and approval of a tablet formulation. Public records do not show that Kioupritzi herself led the FDA submissions.
Sep.22
Product | BAT Expands VELO Travellers’ Collection With Mexico, Spain and Sweden Summer Edition Nicotine Pouches
Product | BAT Expands VELO Travellers’ Collection With Mexico, Spain and Sweden Summer Edition Nicotine Pouches
British American Tobacco (BAT) Global Travel Retail has expanded the VELO Travellers’ Collection with three new Summer Editions: Mexico, Spain and Sweden. Inspired by destination themes, the new nicotine pouch variants are designed for global travel-retail channels. The launch further strengthens VELO’s positioning as a travel-retail exclusive product collection.
Aug.27
As JUUL2 Wins FDA Authorization, Harm Reduction Journal Highlights the Role of Real-World Evidence in Nicotine Product Regulation
As JUUL2 Wins FDA Authorization, Harm Reduction Journal Highlights the Role of Real-World Evidence in Nicotine Product Regulation
A commentary published in the international open-access, peer-reviewed Harm Reduction Journal argues that randomized controlled trials remain central to evaluating smoking cessation efficacy but cannot alone capture real-world uptake, complete switching, longer-term use and population impact of non-combustible nicotine products such as e-cigarettes, heated tobacco and nicotine pouches. The authors frame impact as “reach × efficacy” and call for real-world evidence to complement RCTs. Three days after publication, the FDA authorized three JUUL2 products and highlighted complete switching among adult smokers in explaining its decision, providing a timely regulatory backdrop to the debate.
Sep.08