BLUEHOLE-NEW-CONSUMPTION
17.11.2021 02:50:09 CET | Business Wire | Press release
China’s leading vaping media, Bluehole New Consumption, today published a feature story on global advocacy for tobacco harm reduction prior to WHO FCTC COP9, while atomization offers promising prospects in healthcare and other fields.
Here below is the full article in English:
The Ninth Session of the Conference of the Parties (COP9) to the World Health Organization (WHO) Framework Convention on Tobacco Control (FCTC) took place on November 8-13, 2021. During the conference, the delegates debated over measures to reduce smoking-related death and disease.
According to the earlier announcement of the FCTC Secretariat, in this year’s COP (COP9), evident on vaping and heat-not-burn products will be presented to the Parties, however, no decision will be made until COP10 in 2023.
The WHO FCTC is a legally binding treaty that requires member countries — or Parties — to implement its measures as calls for more rigorous regulations on tobacco marketing and increased taxation of tobacco products, in a bid to reduce tobacco uses and exposures to tobacco smoke from both demand and supply ends.
In fact, the WHO once recognized in 2020, “completely substituting electronic nicotine and non-nicotine delivery systems (EN&NNDS) for combustible tobacco cigarettes reduces users’ exposure to numerous toxicants and carcinogens present in combustible tobacco cigarettes.”
However, in practice, the WHO has rejected reduced-risk products, such as e-cigarettes, as the real-world strategy to improve public health. Instead, the WHO FCTC exhorts its Parties to impose high taxes and bans on all tobacco products, no matter combustible or non-combustible products. The WHO remains doubtful about e-cigarettes and other reduced-risk products, considering them an industry tool to get consumers hooked on nicotine.
In July 2021, the WHO released a report on the global tobacco epidemic 2021. It is the first time that the organization presented data on electronic nicotine delivery systems (ENDS) and argued that ENDS need to be regulated.
Moreover, WHO FCTC COP9 raised more global concerns over biased regulatory guidance, which will undermine vaping’s potential to benefit public health, suggesting a step backward for global public health. For example, in the US, cigarette sales rose in 2020 for first time in two decades. Public health experts warn that House Democrats’ voting on vaping tax without a tax increase in cigarettes will push vapers back to more harmful combustible tobacco.
100 specialists in nicotine science, policy and practice from all over the world has also signed a letter to Parties to the FCTC to encourage WHO to promote the inclusion of tobacco harm reduction into the FCTC. This letter argues that “e-cigarettes are a driver of smoking cessation and tobacco harm reduction presents significant public health opportunities”.
The British Chamber of Commerce of the Philippines (BCCP) has also encouraged the Philippines government to join United Kingdom in accepting a science-based approach in combating smoking problem ahead of the WHO FCTC COP9.
As an advocate for Tobacco Harm Reduction, the U.K government recently announces its plan to integrate medically licensed e-cigarettes into NHS prescription to reduce smoking rates. Since 2014, Public Health England(PHE) has issued a series of reports on latest evidence on the effects of vaping products on smoking cessation. The agency also concluded that e-cigarettes are around 95% less harmful than combustible tobacco.
The global adoption of reduced-risk products, including e-cigarette, for the benefit of public health, is inevitable. Global health regulators should seize the “single biggest public health opportunity’, according to New York University Professor David Abrams.
In addition, the vaping industry players have also been proactively exploring the applications of atomization technology in healthcare and other fields, transforming into broader atomization healthcare and wellness businesses. For example, British America Tobacco’s US bio-tech subsidiary is working on a potential vaccine for COVID-19 while Philip Morris has acquired inhaled-drug firm OtiTopic and asthma inhaler maker Vectura. Committed to building the world’s leading atomization technology platform, SMOORE, the world’s largest vaping manufacturer, is also about to launch its atomized healthcare and beauty technologies in early December.
To read the original article, please visit: https://www.bluehole.com.cn/news/detail/47508
View source version on businesswire.com: https://www.businesswire.com/news/home/20211116006457/en/
About Business Wire
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
Barilla Opens Global Call for Startups Through Good Food Makers 202625.5.2026 11:47:00 CEST | Press release
The program has involved over 1,100 startups across 50+ countries, delivering 26 pilot projects. Barilla Group has opened applications for the 2026 edition of Good Food Makers, its global open innovation program designed to co-develop and test new innovative solutions with startups and innovators inside real industrial environments. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260521973445/en/ Since its launch in 2019, the program has involved more than 1,100 startups from over 50 countries, leading to 26 pilot projects, with over 20 projects currently active thanks to the solutions developed by the program’s alumni. This highlights the program’s role as a concrete platform for industrial scalable innovation. The 2026 edition comes at a pivotal moment for the company, following the launch of BITE (Barilla Innovation & Technology Experience), the new innovation center dedicated to developing the next generation of food prod
JEOL: Sales Launch of the Laser SEM System “LazEdge”25.5.2026 10:16:00 CEST | Press release
JEOL Ltd. (President & CEO: Izumi Oi) has developed the “LazEdge”, an SEM system equipped with a laser processing system, and begins sales on May 25, 2026. Cross-section preparation instruments such as the focused ion beam system (FIB system), are widely used in science and technology fields across research institutes, universities, and industries. In recent years, demand is increasing for a system that can process large-areas at a high speed, while achieving high-quality of the processed surface. “LazEdge” is an instrument integrating JEOL’s SEM with the laser technology proprietary of Hamamatsu Photonics K.K., and enables laser processing inside the specimen chamber of the electron microscope. This system enables high-quality cross-section specimens produced through high-speed, large-area processing to be transferred seamlessly to subsequent analyses, such as SEM observation, elemental analysis, and crystal orientation analysis, without exposure to the external environment. As a resu
TFG-001, A Novel 3D Neural Microtissue Cell Therapy, Demonstrates Superior Functionality and Reinnervation for Parkinson’s Disease25.5.2026 08:00:00 CEST | Press release
TreeFrog Therapeutics, a regenerative medicine biotech company developing next-generation cell therapies, today announced that it will present new preclinical data on TFG-001 at the 7th World Parkinson’s Conference. TFG-001, a 3D neural microtissue cell therapy, demonstrated rapid dopamine release and extensive graft-derived reinnervation across multiple advanced translational Parkinson’s disease models—supporting its potential as a best-in-class candidate. The critical need for reinnervation in Parkinson's disease In Parkinson's disease, an estimated 60–80% of dopaminergic neurons are already lost before motor symptoms even appear. The nigrostriatal pathway degenerates, destroying the essential wiring that connects dopamine-producing neurons to movement control. While chemical dopamine replacements (like levodopa) can manage symptoms, they cannot restore the spatial precision, feedback loops, or dynamic regulation of a healthy brain network. To achieve true functional restoration, it
Galderma Receives U.S. FDA Approval for Differin® Epiduo® Acne Gel Prescription-to-OTC Switch22.5.2026 18:25:00 CEST | Press release
A unique Prescription-to-OTC switch in acne care, this approval expands access to a dermatologist-trusted, prescription-strength treatment for millions of acne sufferers ages 12 years and older Backed by more than 15 years of real-world dermatologist use and a robust clinical research program, this milestone demonstrates the depth of science behind the Differin® and Epiduo® heritage Adapalene plus benzoyl peroxide (0.1/2.5%) was the first FDA-approved, stable, fixed- dose prescription acne treatment to combine of benzoyl peroxide with a retinoid, and is now available over-the-counter The formulation is engineered to target multiple causes of acne more effectively than either of its individual active ingredients alone Galderma (SIX: GALD), the pure-play dermatology category leader, today announced that the United States (U.S.) Food and Drug Administration (FDA) has approved Differin® Epiduo® Acne Gel (Adapalene 0.1% and Benzoyl Peroxide 2.5% Acne Treatment) for over-the-counter (OTC) us
Avanzanite Bioscience’s Partner Agios Announces PYRUKYND® (mitapivat) Approval in the European Union for Adults with Thalassaemia22.5.2026 16:18:00 CEST | Press release
Avanzanite will commercialise and distribute PYRUKYND in Europe under its exclusive agreement with Agios Avanzanite is committed to collaborating with local authorities in the EU to enable access to PYRUKYND for adult patients with thalassaemia Avanzanite Bioscience B.V., a rapidly growing commercial-stage European specialty pharmaceutical company focused on rare diseases, today reported that its partner, Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), a commercial-stage biopharmaceutical company headquartered in Cambridge, Massachusetts focused on delivering innovative medicines for patients with rare diseases, announced that the European Commission has granted marketing authorisation for PYRUKYND® (mitapivat), an oral pyruvate kinase (PK) activator, in adults for the treatment of anaemia associated with transfusion-dependent and non-transfusion-dependent alpha- or beta-thalassaemia, with an orphan medicinal product designation. This press release features multimedia. View the full releas
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom
