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Time of India
01-07-2025
- Health
- Time of India
‘Pillars of humanitarian service': City honours health workers with events
Bhopal: Medical institutions observed National Doctors' Day with events recognizing physicians' contributions to society. Bhopal Memorial Hospital and Research Centre (BMHRC), Gandhi Medical college (GMC) and AIIMS Bhopal all held ceremonies and tributes. BMHRC's 25th anniversary coincided with the day. Bhopal MP Alok Sharma inaugurated the silver jubilee Year, planted trees and revealed a new echocardiography machine for heart disease detection. He also unveiled a commemorative logo and portraits of ancient Indian medical figures Acharya Charaka and Acharya Sushruta. Sharma advocated for BMHRC to become a medical college and establish a general medicine department. He pledged support for future proposals to improve services. BMHRC director (in-charge) Dr Manisha Srivastava reported that currently BMHRC has a record high of 183 doctors. At GMC, Progressive Medical Teachers Association (PMTA) hosted an event recognizing doctors from Madhya Pradesh. MP deputy CM and health minister, Rajendra Shukla was the chief guest. Principal secretary health and medical education Sandeep Yadav also attended. by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like Giao dịch vàng CFDs với sàn môi giới tin cậy IC Markets Tìm hiểu thêm Undo PMTA recognized Dr Leela Joshi (Ratlam), Dr H.H. Trivedi (Bhopal), Dr M.K. Jain (Rewa), Dr Bhanu Pratap Dubey (Bhopal), Dr Y.R. Yadav (Jabalpur), Dr Sanjeev Gaur (Bhopal), Dr Manohar Bhandari (Indore) and Dr Katyayan Mishra (Ujjain). PMTA president Dr Rakesh Malviya stated the association's commitment 'to cooperating with the state govt to improve public health indicators'. Over 500 medical professionals attended, including faculty from GMC. AIIMS Bhopal faculty and staff reaffirmed their commitment to ethical service and patient care. Institute director Dr Ajai Singh said that doctors are more than medical professionals, they are pillars of humanitarian service. The gathering also honored Dr Bidhan Chandra Roy, eminent physician, freedom fighter, and statesman—is the inspiration behind India's National Doctors' Day, observed annually on July 1st in honour of his remarkable legacy. Get the latest lifestyle updates on Times of India, along with Doctor's Day 2025 , messages and quotes!
Time Business News
04-06-2025
- Health
- Time Business News
Online News Spotlight: Global Vape Kit Policy Changes Shaping the Future of Vaping
The global landscape of vaping regulations is shifting rapidly as governments and health authorities respond to rising concerns over youth vaping, product safety, and public health implications. In recent months, online news platforms have been abuzz with updates about vape kit policy changes in various parts of the world. These updates are shaping consumer behavior, impacting manufacturers, and drawing strong reactions from advocacy groups and health officials alike. In this blog, we'll explore the major policy shifts making headlines across continents, the motivations behind these changes, and the broader implications for the vaping industry. In today's world, ensuring access to pure and safe drinking water is essential for health and well-being. Modern filtration technology has made it easier to remove contaminants and improve water quality effectively. Among the latest innovations, the hayati pro ultra 25000 stands out for its high efficiency and reliability. Designed to handle large volumes of water, it combines advanced filtration methods to eliminate impurities and harmful substances. This system not only provides clean water but also supports sustainable usage with durable components. Perfect for both residential and commercial settings, it represents a significant step forward in water purification technology. In the United States, the Food and Drug Administration (FDA) has intensified its crackdown on unauthorized vape products. Following the ongoing scrutiny over flavored e-cigarettes and their role in youth vaping epidemics, the FDA has issued warning letters to several manufacturers and retailers. Recent online reports highlight that the agency is actively seeking to remove from the market all vape kits that haven't undergone its premarket tobacco product application (PMTA) process. In particular, the FDA is targeting disposables and fruit-flavored products that are appealing to minors. The heightened regulation has triggered widespread debate. Public health experts support the move, citing concerns over increasing teen nicotine addiction. On the other hand, adult users and harm reduction advocates argue that overregulation may inadvertently push people back to smoking traditional cigarettes. News outlets covering these stories emphasize the delicate balance regulators must strike between protecting youth and supporting smokers trying to quit through vaping. Across the Atlantic, the UK government is planning to introduce a new vape tax as part of its broader anti-smoking strategy. According to online reports from major British media outlets, the proposed legislation includes restrictions on vape flavors, packaging designs, and a new excise tax on vape liquids. The move has sparked a wave of public feedback and concern among vaping communities, particularly because the UK has traditionally been more vape-friendly compared to other nations. British health authorities have promoted vaping as a smoking cessation tool for years. However, rising rates of youth experimentation and illegal sales of high-nicotine devices have forced the government to reconsider its approach. Online news articles highlight how the proposed policies aim to reduce underage access while maintaining support for adult smokers. Still, critics warn that heavy-handed measures could erode public trust and damage one of the country's most successful harm reduction strategies. Australia continues to lead with one of the strictest vaping policies globally. As of recent updates, vape kits containing nicotine can only be accessed through a doctor's prescription. This policy has been in place for a while, but online news platforms report that enforcement has intensified in 2025. Border seizures of illegal vape imports have increased, and authorities are cracking down on retailers violating the rules. Online media coverage from Australian health officials points to youth protection and addiction prevention as the primary goals. However, public health advocates and medical professionals remain divided. Some argue that restricted access is crucial to curbing rising youth vaping rates, while others say it places unnecessary burdens on adults seeking safer alternatives to smoking. Online discussions often focus on how the black market is thriving under the current framework, undermining the policy's original intent. New Zealand's vaping policy has traditionally favored a balanced, harm-reduction approach. However, online news sources reveal that the government is now reviewing its regulatory stance in light of growing public health concerns. Changes being considered include limiting the types of vape flavors allowed, enforcing stricter advertising rules, and introducing tougher penalties for retailers who sell to minors. Health officials in New Zealand still support vaping as a tool to help people quit smoking, a position echoed by many online editorials and expert interviews. However, policymakers are now more cautious, especially given data suggesting a rise in youth vaping prevalence. The upcoming policy review is expected to incorporate insights from both public health research and community consultations. The European Union is witnessing a patchwork of vape regulations across its 27 member countries. Online news outlets are closely monitoring efforts by the European Commission to update the Tobacco Products Directive (TPD), which governs the sale and marketing of vape products. New proposals are expected to address nicotine limits, product labeling, cross-border sales, and environmental concerns related to disposable devices. EU-based news coverage indicates a strong push from health NGOs to introduce plain packaging and flavor bans, particularly for fruity and sweet vape kits. However, industry voices are cautioning against policies that might stifle innovation or limit access to potentially life-saving alternatives. The conversation online also includes growing concern about illicit trade and how uneven enforcement across member states can compromise regulatory goals. In Canada, several provinces have moved ahead with their own flavor bans, sparking nationwide discussion. Online news reports confirm that provinces like British Columbia and Nova Scotia have restricted or banned the sale of flavored vape products, citing their appeal to young users. Health Canada is also reportedly considering national regulations to align with these provincial measures. Online media commentary shows a growing divide between federal and provincial policies, with some stakeholders calling for a more unified approach. Youth vaping statistics have been central to the debate, and public reactions vary widely. Some applaud the bans as a necessary step, while others argue they could reduce smoking cessation success rates. The story continues to evolve as lawmakers seek a compromise that supports both public health and adult smokers. The vaping regulatory environment in Asia is highly diverse, as highlighted by various online news platforms. Countries like Japan and South Korea have adopted relatively permissive policies toward heat-not-burn tobacco products but remain cautious about nicotine vapes. Meanwhile, nations such as India and Thailand have implemented outright bans on e-cigarettes, citing public health risks and lack of long-term safety data. In China, the world's largest manufacturer of vape products, the government has introduced strict new rules governing product standards, marketing, and domestic sales. Online coverage reveals that these changes are intended to align the vape industry with traditional tobacco controls, a move that significantly affects global supply chains. The Asian market's varied regulatory stances continue to influence how international companies navigate compliance and innovation. Across the globe, the vaping industry is grappling with the implications of these policy shifts. Online news reports frequently cover how manufacturers are adjusting product lines, reformulating flavors, and investing in compliance infrastructure. Meanwhile, consumers are expressing frustration over reduced access to preferred products and confusion about new laws. Some online stories spotlight the rise of advocacy groups pushing back against restrictive measures, arguing for evidence-based policies that prioritize harm reduction. Others focus on the booming black market and how regulatory gaps are being exploited. For consumers, especially those using vaping as a smoking cessation aid, these changes can mean fewer choices and more uncertainty. As online news coverage illustrates, vape kit policy changes are unfolding rapidly across the world, reflecting broader societal tensions between innovation, public health, and personal freedom. Governments are increasingly walking a tightrope—balancing the need to protect youth while enabling smokers to access less harmful alternatives. Whether through outright bans, strict regulation, or supportive harm-reduction models, the direction of policy will continue to evolve in response to public opinion, emerging science, and industry developments. For vape users, manufacturers, and policymakers alike, staying informed through credible news sources is essential. The future of vaping remains uncertain, but one thing is clear: the global regulatory landscape will continue to be a hotbed of debate, transformation, and innovation in the months and years ahead. TIME BUSINESS NEWS
Associated Press
04-06-2025
- Business
- Associated Press
IKE Tech's PMTA for First-Ever Standalone Age-Gating System at Point of Use Accepted for FDA Review Just One Month After Submission
The organization's blockchain technology is set to redefine public health safeguards and help end youth vaping for good. LOS ANGELES, June 4, 2025 /PRNewswire/ -- IKE Tech LLC ('IKE Tech'), a leading innovator at the intersection of Internet of Things (IoT), identity verification, and tokenization technology, has received an Acceptance Review letter from the U.S. Food and Drug Administration (FDA) for its Premarket Tobacco Product Application (PMTA), just one month after submission on April 26. This marks the first time the FDA has proceeded with a PMTA for a standalone, interoperable age-gating component providing real-time age verification at the point of use for electronic nicotine delivery systems (ENDS). Potentially compatible with all ENDS devices, the IKE system integrates a Bluetooth Low Energy (BLE) System-on-a-Chip with the smartphone-enabled IKE Mobile Application, enabling secure, continuous age and identity verification. In a multi-center Human Factors Validation Study, submitted with the PMTA, 0% of underage users were able to activate a device, showcasing the reliability of IKE Tech's blockchain-based technology in safeguarding public health. Receipt of the FDA's Acceptance letter confirms that the IKE Tech PMTA meets regulatory requirements to be accepted and moves the application into the FDA's filing review phase. John Patterson, President of IKE Tech, said: 'Receiving the Acceptance Review letter from the FDA faster than most applications is a major milestone for IKE Tech and a promising step forward for public health in the ENDS category. By leveraging Bluetooth, biometrics, and blockchain, we're unlocking a new era of vaping – one that gives regulators and manufacturers the power to lock out youth and ensure adult-only access. We're proud to be leading the way with a secure, scalable solution that could become the new baseline for responsible product access in the US and beyond.' – ENDS – Notes to Editors: Human Factors Study Design and Key Results Conducted with 102 participants (51% male, 49% female, aged 18–67 across race/ethnic demographics), the study simulated real-world use of the IKE system. Participants downloaded the app, verified their age, paired with a test device and interacted with BLE-based access controls including biometric activation. Key performance highlights: Devices could only be activated after successfully passing the age-gating process. Demographic data (age, race/ethnicity, gender) was accurately verified in all cases. The results confirm the IKE System's ability to reduce user error and prevent underage access. About IKE Tech IKE Tech LLC ('IKE Tech') is pioneering real-time age and identity verification at the point of use, helping to safeguard access to age-restricted products. A leading innovator at the intersection of Internet of Things (IoT), identity verification (IDV), and tokenization technology, IKE Tech has developed an industry-first, scalable age-gating component that provides continuous, real-time verification for electronic nicotine delivery systems (ENDS) and other restricted consumer products. IKE Tech's interoperable Bluetooth Low Energy (BLE) System-on-a-Chip, powered by a user-friendly mobile app available on iOS and Android, integrates seamlessly into ENDS devices, giving manufacturers and regulators a flexible, future-proofed solution to combat underage vaping and illicit markets. By setting the new standard for responsible, adult-only access, IKE Tech is helping eliminate youth vaping for good. Media contact [email protected] View original content: SOURCE IKE Tech LLC
Yahoo
04-06-2025
- Business
- Yahoo
IKE Tech's PMTA for First-Ever Standalone Age-Gating System at Point of Use Accepted for FDA Review Just One Month After Submission
The organization's blockchain technology is set to redefine public health safeguards and help end youth vaping for good. LOS ANGELES, June 4, 2025 /PRNewswire/ -- IKE Tech LLC ("IKE Tech"), a leading innovator at the intersection of Internet of Things (IoT), identity verification, and tokenization technology, has received an Acceptance Review letter from the U.S. Food and Drug Administration (FDA) for its Premarket Tobacco Product Application (PMTA), just one month after submission on April 26. This marks the first time the FDA has proceeded with a PMTA for a standalone, interoperable age-gating component providing real-time age verification at the point of use for electronic nicotine delivery systems (ENDS). Potentially compatible with all ENDS devices, the IKE system integrates a Bluetooth Low Energy (BLE) System-on-a-Chip with the smartphone-enabled IKE Mobile Application, enabling secure, continuous age and identity verification. In a multi-center Human Factors Validation Study, submitted with the PMTA, 0% of underage users were able to activate a device, showcasing the reliability of IKE Tech's blockchain-based technology in safeguarding public health. Receipt of the FDA's Acceptance letter confirms that the IKE Tech PMTA meets regulatory requirements to be accepted and moves the application into the FDA's filing review phase. John Patterson, President of IKE Tech, said: "Receiving the Acceptance Review letter from the FDA faster than most applications is a major milestone for IKE Tech and a promising step forward for public health in the ENDS category. By leveraging Bluetooth, biometrics, and blockchain, we're unlocking a new era of vaping – one that gives regulators and manufacturers the power to lock out youth and ensure adult-only access. We're proud to be leading the way with a secure, scalable solution that could become the new baseline for responsible product access in the US and beyond." – ENDS – Notes to Editors: Human Factors Study Design and Key Results Conducted with 102 participants (51% male, 49% female, aged 18–67 across race/ethnic demographics), the study simulated real-world use of the IKE system. Participants downloaded the app, verified their age, paired with a test device and interacted with BLE-based access controls including biometric activation. Key performance highlights: 100% of users (n=101) successfully completed age verification 0% of underage users were able to activate a device 100% of devices deactivated after set period of inactivity or loss of Bluetooth signal 91% rated the app "Extremely Easy" or "Very Easy" to use Errors occurred in only 1% of task attempts Devices could only be activated after successfully passing the age-gating process. Demographic data (age, race/ethnicity, gender) was accurately verified in all cases. The results confirm the IKE System's ability to reduce user error and prevent underage access. About IKE Tech IKE Tech LLC ("IKE Tech") is pioneering real-time age and identity verification at the point of use, helping to safeguard access to age-restricted products. A leading innovator at the intersection of Internet of Things (IoT), identity verification (IDV), and tokenization technology, IKE Tech has developed an industry-first, scalable age-gating component that provides continuous, real-time verification for electronic nicotine delivery systems (ENDS) and other restricted consumer products. IKE Tech's interoperable Bluetooth Low Energy (BLE) System-on-a-Chip, powered by a user-friendly mobile app available on iOS and Android, integrates seamlessly into ENDS devices, giving manufacturers and regulators a flexible, future-proofed solution to combat underage vaping and illicit markets. By setting the new standard for responsible, adult-only access, IKE Tech is helping eliminate youth vaping for good. Media contactiketech@ View original content: SOURCE IKE Tech LLC Sign in to access your portfolio
Associated Press
03-06-2025
- Business
- Associated Press
Ispire-Backed IKE Tech to Present 7th Annual Next Generation Nicotine Delivery USA Conference
Conference Attendance Follows Groundbreaking FDA PMTA Filing for Blockchain-Powered Age-Gating System LOS ANGELES, June 3, 2025 /PRNewswire/ -- Ispire Technology Inc. ('Ispire' or the 'Company') ( NASDAQ: ISPR ), a trailblazer in vaping technology and precision dosing, announced that IKE Tech LLC ('IKE Tech'), a joint venture that includes Ispire as a founding partner, will showcase their technology at the 7th Annual Next Generation Nicotine Delivery USA at the Hyatt Regency in Miami from June 4-5th. This event convenes key business leaders from the FDA, the ENDS (Electronic Nicotine Delivery Systems) sector, and the tobacco industry across the U.S. market to explore strategies for legal compliance and commercial success. The announcement comes on the heels of IKE Tech's historic milestone, in which the joint venture filed a component Pre-Market Tobacco Product Application (PMTA) and Tobacco Product Master File (TPMF) with the U.S. Food and Drug Administration (FDA) for its Bluetooth Low Energy (BLE) System-on-a-Chip. IKE Tech has now received an Acceptance Review letter from the FDA, confirming that their PMTA meets regulatory requirements to be accepted, and moves the application into the FDA's filing review phase. This marked the first-ever complete PMTA submission for a standalone, interoperable, blockchain-enabled age-verification component designed for universal integration across all ENDS devices. Unlike traditional systems that verify age only at the point of purchase, IKE Tech's platform requires continuous, real-time identity verification, offering an unprecedented level of security against underage vaping. IKE has formally requested expedited review of the application, citing its potential to significantly enhance public health. At the conference, John Patterson, senior vice president of International Nicotine at Ispire and president of IKE Tech, will speak on a panel titled " Technology to End Youth Vaping for Electronic Nicotine Delivery Systems,' scheduled for Wednesday, June 4, at 2:00 p.m. In his capacity as President of IKE Tech, Patterson will discuss: To schedule a meeting with John Patterson or other Ispire representatives, please email [email protected]. About IKE Tech LLC IKE Tech LLC is a joint venture comprised of three leading technology and research companies -- Ispire Technology Inc, Touch Point Worldwide Inc. d/b/a Berify, and Chemular Inc. -- dedicated to revolutionizing Identity and Age Verification (IAV) technology solutions. Recognizing the absence of a universal point-of-sale IAV solution and recognition of the need for one, these companies joined forces to create a unique IAV technology component. IKE's mission is to set the gold standard for IAV by (i) permitting access to electronic nicotine delivery systems by authorized adult users while (ii) preventing underage access through a 'plug and play' component compatible across different devices and platforms. About Ispire Technology Inc. Ispire is engaged in the research and development, design, commercialization, sales, marketing and distribution of branded e-cigarettes and cannabis vaping products. The Company's operating subsidiaries own or license more than 400 patents worldwide. Ispire's branded e-cigarette products are marketed under the Aspire name and are sold worldwide (except in the U.S., People's Republic of China and Russia) primarily through its global distribution network. The Company also engages in original design manufacture (ODM) relationships with e-cigarette brands and retailers worldwide. The Company's cannabis products are marketed under the Ispire brand name primarily on an ODM basis to other cannabis vapor companies. Ispire sells its cannabis vaping hardware in the US, Europe and South Africa and it recently commenced marketing activities and customer engagement in Canada and Latin America. For more information, visit or follow Ispire on Instagram, LinkedIn, Twitter and YouTube. Forward Looking Statements This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended ('Securities Act') as well as Section 21E of the Securities Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995, as amended, that are intended to be covered by the safe harbor created by those sections. Forward-looking statements, which are based on certain assumptions and describe the Company's future plans, strategies and expectations, can generally be identified by the use of forward-looking terms such as 'believe,' 'expect,' 'may,' 'will,' 'should,' 'would,' 'could,' 'seek,' 'intend,' 'plan,' 'goal,' 'project,' 'estimate,' 'anticipate,' 'strategy,' 'future,' 'likely' or other comparable terms, although not all forward-looking statements contain these identifying words. All statements other than statements of historical facts included in this press release regarding the Company's strategies, prospects, financial condition, operations, costs, plans and objectives are forward-looking statements. Important factors that could cause the Company's actual results and financial condition to differ materially from those indicated in the forward-looking statements. Such forward-looking statements include, but are not limited to, risks and uncertainties including those regarding: the Company's ability to collect its accounts receivable in a timely manner, the Company's business strategies, the ability of the Company to market to the Ispire ONE™, Ispire ONE's success of meeting its goals, the ability of its customers to derive the anticipated benefits of the Ispire ONE™ and the success of their products on the markets; the Ispire ONE™ proving to be safe, and the risk and uncertainties described in 'Risk Factors,' 'Management's Discussion and Analysis of Financial Condition and Results of Operations,' 'Cautionary Note on Forward-Looking Statements' and the additional risk described in Ispire's Annual Report on Form 10-K for the year ended June 30, 2023 and any subsequent filings which Ispire makes with the U.S. Securities and Exchange Commission. You should not rely upon forward-looking statements as predictions of future events. The forward-looking statements made in the press release relate only to events or information as of the date on which the statements are made in the press release. We undertake no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, after the date on which the statements are made or to reflect the occurrence of unanticipated events except as required by law. You should read this press release with the understanding that our actual future results may be materially different from what we expect. IR Contacts: For more information, kindly contact: Investor Relations Sherry Zheng 718.213.7386 [email protected] KCSA Strategic Communications Phil Carlson 212.896.1233 [email protected] PR Contact: Ellen Mellody 570.209.2947 [email protected] View original content: SOURCE Ispire Technology Inc.
