The Importance of Evidenced-Based Debate on E-Cigarettes

Aug.30.2022
The Importance of Evidenced-Based Debate on E-Cigarettes
eSmoking Institute highlights importance of evidence-based discussions on reducing harm and promoting safer e-cigarettes for smokers.

In public discourse, there is an increasing discussion around reducing the health damages associated with smoking, and further research confirms that approximately 95% of e-cigarettes are less toxic than traditional cigarettes, and may assist with smoking cessation.


Marcin Kozłowski, a member of the management board of the eSmoking Institute, a professional research and development center located in Poznan, emphasized the importance of using modern research techniques for reliable, evidence-based public debates. The institute has been dedicated to expanding its research field and has recently purchased equipment to support advanced technology development, including tools that allow for a wider range of testing of water content in nicotine liquids. The institute has also acquired a modern viscometer for dynamic viscosity testing, which will enable them to broaden the scope of their physical and chemical testing.


The head of eSI spoke about the institute's work, stating that their goal is to develop regulations and standards to help smokers better understand the products available in the market. This will further improve the safety of these products. They are also closely monitoring the research of other leading centers in this field. Most importantly, e-cigarette users can now identify that they are using verified, less harmful products and the institute is pleased that more and more people are gaining knowledge about these products.


Marcin Kozłowski is a member of the management board of the eSmoking Institute/Fot.


What is an electronic cigarette?


This is the idea behind the creation of the product, which does not contain tar substances that are known to cause many smoking-related diseases. It works like an inhaler, providing the body with nicotine through the process of evaporating a liquid (based on glycerin and propylene glycol). Therefore, no tobacco is burned, and the amount of toxic substances released in the aerosol compared to traditional tobacco products such as cigarettes is much lower. Clearly, electronic cigarettes are much less harmful than traditional cigarettes, as our research and independent international studies have shown. M. Kozłowski cited a report from the UK Public Health England, which concluded that 95% of the content in electronic cigarettes is tar-free and therefore less harmful compared to traditional cigarettes.


In this context, we often hear about "harm reduction." What exactly does that mean?


Against the backdrop of policies to reduce the harm caused by smoking, it is worth highlighting the role of electronic cigarettes. Some countries in the world, including New Zealand, the United States, and previously mentioned United Kingdom, have implemented policies suggesting that smokers who are unable to quit should switch to the less harmful alternative of electronic cigarettes, even in the form of prescriptions. Surprisingly, this has yielded impressive results. For instance, research conducted in the United Kingdom shows that as many as 52% of its 3.2 million adult electronic cigarette users have quit smoking. Conversely, Spain reports that nine out of ten electronic cigarette users in their country have either completely quit or significantly reduced their nicotine intake. Therefore we have increasingly strong reasons to believe that policies aimed at reducing harm will produce extremely positive results. However, it should be remembered that the products we use must be thoroughly tested.


What else should we know?


The electronic cigarette market offers a variety of options for users, including open or closed systems that only require the replacement of liquid cartridges, such as the Vuse ePod. In my opinion, it is important that we ensure consumers are unable to alter any aspect of the product, so that it can be thoroughly reviewed for its final formulation and ingredients. If we choose to use open systems, only single-use liquids should be permitted. The concept of the finished product would involve providing a substance that is constrained by the entire testing system with regards to its final formulation.


Statement


This article is compiled from third-party information and is intended for industry communication and learning purposes only.


This article does not represent the views of 2FIRSTS and 2FIRSTS cannot confirm the authenticity or accuracy of the content of this article. The translation of this article is only intended for industry communication and research purposes.


Due to limitations in the level of translation, the compiled article may not fully express the content of the original text. Please refer to the original text for accuracy.


2FIRSTS maintains complete alignment with the Chinese government regarding any domestic, Hong Kong, Macau, Taiwan, or foreign statements or positions.


The copyright of compiled information belongs to the original media and author. If there is any infringement, please contact us for immediate removal.



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.

Trump Picks White House Health Policy Aide Heidi Overton to Lead FDA, Pending Senate Confirmation
Trump Picks White House Health Policy Aide Heidi Overton to Lead FDA, Pending Senate Confirmation
U.S. President Donald Trump has chosen White House health policy aide Heidi Overton to lead the Food and Drug Administration, Bloomberg reported, citing a person familiar with the matter. Overton currently works on health policy at the White House and previously held a senior role at the America First Policy Institute. If confirmed by the Senate, she would take over an FDA that has experienced months of senior-level turnover. The agency regulates products representing roughly one-fifth of U.S. consumer spending, including e-cigarettes, drugs, vaccines and much of the food supply.
News
Aug.19
Exclusive Analysis | Smoore H1 Revenue Rises 19.9% Amid Growth Concentration, Profit Pressure and Slowing Momentum
Exclusive Analysis | Smoore H1 Revenue Rises 19.9% Amid Growth Concentration, Profit Pressure and Slowing Momentum
Smoore’s first-half 2026 revenue rose 19.9%, but the results revealed growing structural risks beneath the headline growth. Heat-not-burn contributed about 61% of incremental revenue and remains driven largely by one core customer, while traditional vaping markets diverged, own-brand growth slowed and China enterprise revenue declined further. Gross profit and adjusted profit lagged revenue growth, while second-quarter revenue growth slowed to about 1.9%, putting greater focus on the quality, concentration and sustainability of Smoore’s expansion.
Capital Markets
Aug.20
Australia Tobacco Tax Debate Spreads Within Labor as NSW Premier Minns Reaffirms Support for a Cut
Australia Tobacco Tax Debate Spreads Within Labor as NSW Premier Minns Reaffirms Support for a Cut
Australia’s tobacco excise debate is increasingly exposing differences within the governing Labor Party. New South Wales Labor Premier Chris Minns reaffirmed on September 8 that he supports reducing tobacco excise, arguing that current tax settings are pushing consumers toward cheaper black-market cigarettes. Federal Health Minister Mark Butler continues to oppose an excise cut, while Treasurer Jim Chalmers and Assistant Treasurer Daniel Mulino have recently stopped short of ruling out future changes. The divergence follows the opposition Coalition’s proposal to cut tobacco excise by 80%.
Sep.08
Pennsylvania Vape Directory Enforcement Starts Oct. 19, Barring Retail Sales of Unlisted Products
Pennsylvania Vape Directory Enforcement Starts Oct. 19, Barring Retail Sales of Unlisted Products
Pennsylvania's Act 57 vape directory regime will reach the end of its 120-day inventory transition period on Oct. 19. Nicotine-containing e-cigarettes intended for retail sale in the state that are not listed on the Attorney General's ENDS directory will then be barred from retail sale and treated as contraband subject to seizure, forfeiture and destruction. Manufacturers face annual product certification, brand- and style-based fees and a minimum $50,000 surety bond, while retailers and wholesalers must source through licensed channels and monitor the directory.
Regulations
Oct.08
Germany Probes 7.6 Million Illegal Vape Case With Estimated €33.3 Million Tax Loss; Four Chinese Manufacturer Employees Under Investigation, Some Packaging in Enforcement Images Resembles FUMOT Products
Germany Probes 7.6 Million Illegal Vape Case With Estimated €33.3 Million Tax Loss; Four Chinese Manufacturer Employees Under Investigation, Some Packaging in Enforcement Images Resembles FUMOT Products
German prosecutors and customs authorities are conducting a criminal investigation into an alleged cross-border organised vape network. Authorities say that between January 2024 and March 2025, four employees of an unnamed Chinese e-cigarette manufacturer allegedly built a network of sales agents and wholesalers that brought more than 7.6 million nicotine disposable vapes into Germany, causing an estimated €33.3 million in excise-tax losses. The manufacturer has not been named. Some products visible in enforcement images have packaging resembling products from FUMOT’s portfolio. European regulatory records from 2024, FUMOT’s public overseas-sales materials and records involving German vape importer and distribution company Zamu-Pro GmbH also show FUMOT/RandM products and German distribution activity during the period covered by the investigation.
Sep.21
UK HMRC Launches Vape Duty Stamps on October 1, Ushering in Supply-Chain Traceability as Chinese Exporters Face New Compliance Hurdles
UK HMRC Launches Vape Duty Stamps on October 1, Ushering in Supply-Chain Traceability as Chinese Exporters Face New Compliance Hurdles
HM Revenue & Customs put the UK's Vaping Products Duty and Vaping Duty Stamps Scheme into effect on October 1. All vaping liquids manufactured in or imported into the UK are now subject to duty at £2.20 per 10ml, regardless of nicotine content. The stamp regime will introduce digital functionality designed to provide traceability throughout the supply chain, with approved manufacturers, importers and warehousekeepers required to report product movements and retailers and consumers eventually able to scan stamps to verify authenticity. China exported $177 million of vape-related products to the UK in August, up 51.4% year over year, increasing the significance of the new compliance regime for China's Shenzhen-centered vape supply chain.
Regulations
Oct.04