Next-Level AML: XBO.com Integrates Elliptic’s Compliance Solution

Next-Level AML: XBO.com Integrates Elliptic’s Compliance Solution

Compliance being a pressing issue, crypto players like XBO.com seek partnerships with top AML solution providers New York, NY – August 20, 2024 – (SeaPRwire) – In the rapidly evolving cryptocurrency landscape, platforms like XBO.com, a leading B2C crypto service, are at the forefront of ensuring secure and compliant trading environments. As the crypto market matures, the “Wild West” days of unregulated financial flows are giving way to a new era where compliance and transparency are paramount. XBO.com is setting the standard by integrating cutting-edge Anti-Money Laundering (AML) solutions to protect its users and foster trust in the digital finance ecosystem. XBO.com recognizes the importance of regulatory compliance in today’s crypto market. To maintain its position as a trusted crypto service, XBO.com has adopted robust AML measures that not only ensure legal operations but also build confidence among users and investors, especially those new to the world of digital currencies. AML and Compliance: Cornerstones of XBO.com’s Strategy As a comprehensive crypto service, XBO.com understands that adherence to AML regulations is essential for the long-term success of any crypto platform. Compliance helps prevent illegal activities such as money laundering, which can undermine the credibility of the entire financial ecosystem. XBO.com is committed to upholding the highest standards of legal compliance, which is crucial for maintaining its reputation as a trustworthy platform in the eyes of both regulators and users. For crypto exchanges like XBO.com, implementing strong AML policies is not just about meeting regulatory requirements—it’s about safeguarding the entire crypto market from exploitation by bad actors. By ensuring full compliance with global and local regulations, XBO.com reinforces its commitment to transparency and user protection, making it a go-to platform for both seasoned and novice crypto enthusiasts. XBO.com: A Model of Compliance and User-Centric Innovation While many crypto platforms strive to meet legal requirements, XBO.com goes above and beyond by actively seeking out partnerships with industry leaders in compliance technology. This proactive approach ensures that XBO.com remains at the cutting edge of security and user protection. Emerging as a leader in the crypto exchange sector, XBO.com offers a user-friendly and innovative platform that has evolved into a full-fledged crypto ecosystem. XBO.com is not just a trading platform; it is a comprehensive service where users can access a wide range of features, from spot trading to earning interest on digital assets. The platform’s intuitive design and commitment to accessibility are encapsulated in its motto: “Crypto. Made for everyone.” This philosophy, combined with rigorous compliance measures, sets XBO.com apart in a highly competitive market. Elevating AML Standards: XBO.com Partners with Elliptic In its quest to achieve the highest standards of compliance, XBO.com has partnered with Elliptic, a globally recognized leader in AML and compliance technology for the crypto industry. This strategic alliance highlights XBO.com’s unwavering dedication to lawfulness and user safety. By leveraging Elliptic’s advanced blockchain analytics, XBO.com can detect and prevent illicit activities, ensuring that all transactions on the platform are secure and compliant with global standards. Elliptic provides a comprehensive suite of services that enhance XBO.com’s ability to monitor transactions and identify potential risks. From Wallet Screening and Transaction Monitoring to Crypto Investigations, Elliptic’s tools empower XBO.com to maintain the highest levels of compliance and user protection. This partnership not only strengthens XBO.com’s security infrastructure but also positions the platform as a leader in the fight against money laundering and other financial crimes. Maximizing User Benefits Through Strategic Partnerships By integrating Elliptic’s state-of-the-art AML solutions, XBO.com offers its users an unparalleled level of security and compliance from the moment they join the platform. This collaboration allows XBO.com to implement cutting-edge tools without the delays associated with developing an in-house system, ensuring that users benefit from the highest standards of protection and trust. XBO.com’s decision to partner with an industry leader like Elliptic underscores its commitment to providing a secure and compliant trading environment. This move not only enhances user trust but also solidifies XBO.com’s reputation as a responsible and forward-thinking crypto service. Building Trust and Transparency in the Crypto Industry As the cryptocurrency industry continues to evolve, partnerships like the one between XBO.com and Elliptic are essential for advancing regulatory standards and building trust among users and the broader public. XBO.com is leading by example, showing that a commitment to compliance and transparency is key to the future success of the crypto market. By prioritizing legal standards and integrating the best available technologies, XBO.com is setting a benchmark for other crypto platforms to follow. This dedication to legality and transparency will contribute to a safer and more reliable future for all users in the cryptocurrency space. As the industry matures, XBO.com’s partnership with Elliptic will play a crucial role in ensuring that the platform remains a trusted and secure environment for all its users, ultimately helping to shape the future of digital finance. Media Contact Brand: XBO Contact: Media team Website: https://www.xbo.com SOURCE: XBO The article is provided by a third-party content provider. SeaPRwire ( https://www.seaprwire.com/ ) makes no warranties or representations in connection therewith. Sectors: Top Story, Corporate News SeaPRwire provides real time press release distribution for companies and organizations to 6,500+ media outlets & 3.5 million professional desktops in 90 regions. It distributes press releases in different languages, including: IndonesiaFolk, IndoNewswire, SEATribune, IDNewsZone, LiveBerita, DailyBerita, TaiwanPR, SinchewBusiness, AsiaEase, BuzzHongKong, SingapuraNow, TIHongKong, TaipeiCool, TWZip, AsiaFeatured, dePresseNow, THNewson, KULPR, VNFeatured, MENAEntry, HunaTimes, DubaiLite, ArabicDir, BeritaDaring, TekanAsia, JamKopi ...
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China Medical System (00867) Released its 2024 Interim Results:Steady Increase in Revenue and Profit Compared with 2H 2023

CMS enters the “New Product Era” driven by exclusive and innovative products, with exclusive and innovative drugs revenue accounts for over 56%. SHENZHEN, CHINA – August 15, 2024 – (SeaPRwire) – On August 15, 2024, China Medical System Holdings Limited (“CMS” or the “Company”) released its 2024 interim results announcement, with a steady increase in overall revenue and profit for the period compared to the second half (2H) of 2023. In the first half (1H) of 2024, the Company recorded a turnover of RMB3,611.1 million, representing a decrease of 21.7% compared with 1H 2023, an increase of 6.1% compared with 2H 2023. In the case that all medicines were directly sold by the Company, the turnover was RMB4,287.5 million, representing a decrease of 22.6% compared with 1H 2023, an increase of 8.9% compared with 2H 2023; Among which, the total revenue of non-National VBP exclusive products and innovative products was RMB2,404.7 million, accounting for 56.1% of CMS’s revenue in the case that all medicines were directly sold by the Company. Profit for the period was RMB903.4 million, representing a decrease of 52.8% compared with 1H 2023, a substantial increase of 92.8% compared with 2H 2023. The year 2024, not only marks the first year of the commercialization of CMS’s innovative products, but also a crucial point for the release of National Volume Based Procurement (“National VBP”) impact on its financial performance. Deanxit entered the seventh batch of National VBP in November 2022, Plendil and Ursofalk entered the eighth batch of National VBP in July 2023, and none of the three original drugs were selected, which had a negative impact on the Company’s business performance. In 1H 2024, the Company’s overall performance showed a growth trend compared with 2H 2023, indicating that CMS has basically digested the impact of National VBP and successfully entered the “New Product Era” where non-national VBP exclusive products and innovative products drive its growth. With the approval for marketing of LUMEBLUE (Methylthioninium Chloride Enteric-coated Sustained-release Tablets) in June and METOJECT (Methotrexate Injection)’s additional indication of active rheumatoid arthritis (RA) in adults in July this year, CMS’s innovative drug portfolio in the commercialization stage has expanded into 5 products (including 6 indications); simultaneously with a rich and differentiated innovative pipeline reserve. Gathering the power of innovation and riding the momentum of development, CMS is comprehensively shaping new drivers for development with a healthier product structure, further opening up a new cycle of quality development. The “Collaborative and In-house” dual-engine R&D model drives the simultaneous improvement in quantity and quality of the pipeline, accelerating the transformation of innovative biotechnology A profound innovative drug R&D pipeline is an important driving force for the long-term development of CMS. The Company adheres to the purpose of innovation for meeting the unmet clinical needs and solving the difficulties of patient medication, and promotes innovation development through a two-wheel drive of “Collaborative R&D and In-house R&D”, continuously deploying FIC (first-in-class) and BIC (best-in-class) innovative products, and enhancing the capabilities and efficiency of research and clinical development to achieve a rapid transformation of scientific outcomes into social and commercial values. As of now, CMS’s innovative product portfolio approved for marketing in China has been expanded into 5 products (including 6 indications), among which, 4 innovative drugs (VALTOCO, ILUMETRI, METOJECT – psoriasis indication, VELPHORO) have been included in the National Reimbursement Drug List (NRDL) and entered large-scale clinical application; also, CMS newly added LUMEBLUE and METOJECT (RA), for being approved for marketing in China recently. CMS has also steadily advanced the clinical development of innovative products. Currently, Desidustat Tablets is under NDA review in China; Also, a total of about 10 projects have been prepared/launched for their registrational clinical trials, mainly randomized controlled trials (RCT). At the same time, the Company had continued to strengthen basic research and independent innovation capabilities, and successfully promoted more than 10 in-house R&D projects, among which, three innovative drugs (VEGFA/ANG2 Tetravalent Bispecific Antibody, Highly Selective TYK2 Inhibitor CMS-D001 Tablets, and GnRH Receptor Antagonist CMS-D002 Capsules) have entered the clinical development stage. In addition, the Company’s innovative pipeline has continued to expand. CMS Skinhealth collaborated with Incyte once again, and has obtained exclusive license to research, develop, register and commercialize povorcitinib, a selective oral small-molecule JAK1 inhibitor, in countries/territories including Mainland China, Hong Kong, Macau, Taiwan Region and 11 Southeast Asian countries. This further enriched the product portfolio of CMS Skinhealth in the treatment of vitiligo and other immune-mediated dermatology diseases. Subsequently, CMS will continue to produce innovative products with higher efficiency and more controllable costs every year, accelerating the release of innovative value and embracing quality and sustainable performance growth through a healthy product structure dominated by non-National VBP exclusive products and innovative products. Successful commercialization system releases the clinical value of innovative products in an efficient and collaborative manner After 32 years of deep cultivation in specialty therapeutical fields, successful commercialization capability is one of CMS’s core competitiveness. By continuously reinforcing and integrating its commercialization platform, it has achieved in-depth development of its three major business segments including cardio-cerebrovascular/gastroenterology, dermatology, and ophthalmology, and expanded its boundaries in related fields. Additionally, the Company established a highly qualified, professional promotion team with strong execution, as well as extensive channel and resource coverage, which has laid a solid foundation for the rapid market entry and brand building of its innovative products. Four innovative drugs of CMS have entered large-scale clinical applications, covering various disease fields such as central nervous system, dermatology, nephrology, and gastroenterology, and developed synergistically with the existing marketed products in promotion team and channels. Meanwhile, leveraging on the opportunity of being included in the NRDL, CMS is advancing hospital development, brand building, real world studies and medically-driven academic promotion. CMS is improving patients’ accessibility to innovative drugs with the help of patient aid and disease knowledge popularization programs, promoting the release of products’ clinical value. The Dermatology and Medical Aesthetic Business “CMS Skinhealth” regards dermatology prescription products as its core, and extends to light medical aesthetic products and dermatology-grade skincare products, continuously improving the construction of a full life-cycle skin-health management platform covering dermatological treatment, skincare, and medical aesthetics through internal development and external collaboration. In terms of clinical development of dermatology prescription drugs, CMS has completed the Pivotal Real World Study for ruxolibinib cream in vitiligo, and is advancing the registration application process in Mainland China. At the same time, it has continuously complemented the regenerative light medical aesthetic portfolio, among which the China’s medical device registration application of the Poly-L-lactic Acid Microparticle Filler Injection has been accepted by the NMPA during the Reporting Period; and the Company has newly obtained exclusive licenses of three regenerative light medical aesthetic products (Polycaprolactone Microsphere Gel for injection, Calcium Hydroxylapatite Microsphere Gel for injection, and Decellularized Extracellular Matrix Implant), which are currently under the registrational clinical trial stage in China. The results announcement shows that, as of the end of June, the promotion network of CMS has covered over 55,000 hospitals and medical institutions, and approximately 280 thousand retail pharmacies in China. Leveraging the accumulated advantages in cardio-cerebrovascular, gastroenterology, central nervous system, nephrology, ophthalmology, dermatology and other specialty therapeutical fields, CMS steadily releases the scale effect of its specialty businesses, and builds high competition barriers, creating broad commercial potential for its innovative products and exclusive products. Drawing up the internationalization layout to gather momentum for the incremental market Integrating the advantageous resources of the Company, its Southeast Asia business “Rxilient Health”, shares and expands the successful experience of CMS gained from the China market, as well as global quality products and innovative technological resources, into the Southeast Asia market. This accelerates the improvement of the platform integrating “R&D, manufacture, and commercialization” of the Southeast Asia business, empowering Chinese and global pharmaceutical companies to implement the “overseas development” strategy, and also opening up a larger space for incremental development opportunities for CMS. As of the end of June, Rxilient Health has established a competitive product portfolio with more than ten differentiated products, covering therapeutic areas such as oncology, central nervous system, autoimmune, dermatology, and ophthalmology, etc. Rxilient Health is accelerating the relevant work on the market registration processes in Southeast Asian countries for innovative pipeline products, such as ruxolitinib cream, Methylthioninium Chloride Enteric-coated Sustained-release Tablets, and Diazepam Nasal Spray, etc. Furthermore, Rxilient Health collaborated with Junshi Biosciences to promote the registration process of toripalimab (anti-PD-1 monoclonal antibody) in multiple countries in Southeast Asia, aiming to benefit local cancer patients as soon as possible. In December last year, the Company and Rxilient Health joined hands with Pharmaron and other partners to complete the purchase of the Singapore manufacturing plant. This year, all relevant parties have been orderly advancing a series of work for the Singapore manufacturing plant, including equipment testing, quality verification, and production quality system certification, etc., so as to accelerate the CDMO business development, and to optimize the Company’s overseas supply chain and manufacturing capabilities. The business layout will further facilitate more inter-industry cooperation between CMS and global partners in the future, thus jointly building a win-win medical innovation ecosystem with mutual benefits. Conclusion Since its establishment in 1992, CMS has followed the development pattern of the industry and has promoted three significant strategic transformations successfully with a forward-looking vision. The Company started as an agent of imported original drugs, gradually developed to control the rights of original/exclusive products, and then achieved a comprehensive innovative transformation. Each step of the transformation is in sync with the industry development trends. CMS steadily aims towards the ultimate goal, and constantly builds up its strength and resilience to persist through the industry development cycle. With the gradual release of the impact of national VBP on its financial performance, CMS has been transforming into a brand-new company. While embracing the innovation achievements in each stage, CMS is fully prepared for a sustainable and healthier development in the future. About CMS CMS is a platform company linking pharmaceutical innovation and commercialization with strong product lifecycle management capability, dedicated to providing competitive products and services to meet unmet medical needs. CMS focuses on the global first-in-class (FIC) and best-in-class (BIC) innovative products, and efficiently promotes the clinical research, development and commercialization of innovative products, enabling the continuous transformation of scientific research into clinical practices to benefit patients. CMS deeply engages in several specialty therapeutic fields, and has developed proven commercialization capabilities, extensive networks and expert resources, resulting in leading academic and market positions for its major marketed products. CMS continues to promote the in-depth development of its advantageous specialty fields and expand business boundaries. While strengthening the competitiveness of the cardio-cerebrovascular/gastroenterology business, CMS independently operates its dermatology and medical aesthetics business, and ophthalmology business, aiming to gain leading positions in specialty therapeutic fields, whilst enhancing the scale and efficiency. At the same time, CMS has expanded its business territory to the Southeast Asian market, striving to become a “bridgehead” for global pharmaceutical companies to enter the Southeast Asian market, further escorting the sustainable and healthy development of the Group. CMS Disclaimer and Forward-Looking Statements This press release is not intended to promote any products to you and is not for advertising purposes. This press release does not recommend any drugs, medical devices and/or indications. If you want to know more about the diagnosis and treatment of specific diseases, please follow the opinions or guidance of your doctor or other medical and health professionals. Any treatment-related decisions made by healthcare professionals should be based on the patient’s specific circumstances and in accordance with the drug package insert. This press release which has been prepared by CMS does not constitute any offer or invitation to purchase or subscribe for any securities, and shall not form the basis for or be relied on in connection with any contract or binding commitment whatsoever. This press release has been prepared by CMS based on information and data which it considers reliable, but CMS makes no representation or warranty, express or implied, whatsoever, and no reliance shall be placed on, the truth, accuracy, completeness, fairness and reasonableness of the contents of this press release. Certain matters discussed in this press release may contain statements regarding the Group’s market opportunity and business prospects that are individually and collectively forward-looking statements. Such forward-looking statements are not guarantees of future performance and are subject to known and unknown risks, uncertainties and assumptions that are difficult to predict. Any forward-looking statements and projections made by third parties included in this press release are not adopted by the Group and the Company is not responsible for such third-party statements and projections. Media Contact Brand: China Medical System Holdings Ltd. Contact: CMS Investor Relations Email: ir@cms.net.cn Website: https://web.cms.net.cn/en/home/ Source: China Medical System Holdings Ltd.
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An Asian Company Achieves Breakthrough in the Key Technology of Ac-225 Preparation

An Asian Company Achieves Breakthrough in the Key Technology of Ac-225 Preparation

PanMediso Holdings’ international team completes core technology verification for mass production of Ac-225 London, UK – August 15, 2024 – (SeaPRwire) -PanMediso Holdings (Shenzhen) Limited, with the collaborative efforts of its international team and under the witness of authoritative experts, has announced a breakthrough in the key production technology for the medical isotope Ac-225 at a conference held in August, 2024,in London, UK. This core technology has been rigorously validated by a well-known research university in the UK, marking a significant milestone for PanMediso in the scale-up and commercial production of Ac-225. (Key members of the PanMediso Holdings’ international team at the Royal Academy of Engineering) PanMediso is a leading global enterprise in the research, production, and sale of medical isotopes Ac-225 and Ge-68. The company’s first phase focuses on addressing the technological and capacity bottlenecks associated with the long-term reliance on imported medical isotopes in China, aiming for realizing the full process flow of Ac-225 and Ge-68 in China. (PanMediso Holdings’ team meeting on the Technology Validation result) The company’s team comprises top experts in nuclear medicine from various countries, including fellows from the Royal Academy of Engineering and the Royal Society of London, a nuclear fuel expert from the UK government, the former chief scientist from a Canadian nuclear laboratory, and authoritative experts and professors from institutions such as Tsinghua University, Imperial College London, Hong Kong Polytechnic University, Shenzhen University, and Southwest Medical University. They are dedicated to research and clinical applications of radioactive isotopes and nuclear medicine. (PanMediso Holdings Team from left to right:Academician Robin Grimes, Chair of the Joint Technical Committee, Academician Andrew Carlick,CEO UK side, Mr. Leo Dang, CEO China side, Mr. Ivan Fu, Chairman of the Board of Directors) Ac-225 is considered one of the most promising therapeutic isotopes in clinical applications. Currently, dozens of Ac-225 drug pipelines are in clinical research stages worldwide, aiming for the treatment of various cancers including prostate cancer, neuroendocrine tumors, non-small cell lung cancer, breast cancer, and multiple solid tumors. Ac-225 has demonstrated excellent therapeutic effects in clinical research and treatment applications. It not only improves patient survival rates and treatment efficacy while reducing side effects but also lowers medical costs. As one of the most promising and highly anticipated medical isotopes, it is in high demand globally. However, only a few advanced teams outside China master the key production technologies for Ac-225, which involves a complex series of nuclear reactions and separation processes, resulting in a highly limited supply and severe long-term resource shortages. The increasing clinical research and treatment needs both domestically and internationally have exacerbated the shortage. PanMediso’s efforts to bridge this significant supply gap have garnered global attention and will effectively support further exploration of new cancer treatments. This dual value underscores PanMediso Holding’s great commitment to advancing global health through technological innovation and international collaboration, with a steadfast goal of contributing to the community with a shared future of mankind. Academician Andrew Carlick, Co-Founder of PanMediso Holdings, snd Director & CEO on UK side, stated, “The cyclotron-based Ac-225 technology employed by PanMediso Holding is highly mature and has been validated by institutions. As the result of our years of wisdom and resources, it features the advantages such as high purity, high yield, low radiation, and minimal raw material loss, and will play a significant role in cancer treatment. With the combined efforts of our international team, we will continue to advance nuclear medicine technology.” Mr. Leo Dang, Co-Founder of PanMediso Holdings, snd Director & CEO on China side, commented, “PanMediso Holdings will continue to focus on technological and process innovations and plans to further expand the application fields of medical isotopes such as Ac-225 and Ge-68. We aim to provide a comprehensive solution from raw materials to finished products, from research to scaling, and to commercial-level production. We are building a complete technological platform for nuclear medicine, covering isotope production, core equipment research and development, nuclear drug RXO, next-gen diagnostic devices and AI+TAT. While intensifing our research and development strength for radiopharmaceuticals, we keep advancing the clinical translation and application of world-leading technologies, contributing PanMediso Holdings Power to scientific research and healthcare.” Contact Us Company: PanMediso Holdings (Shenzhen) Limited Contact: Claire Zhao Email: pchl@panmedisoholdings.com Website: http://panmedisoholdings.com
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Kess Energy – Kess Energy Chairman Announces Purchase of 200,000 Shares

Brasilia, Brazil – August 14, 2024 – (SeaPRwire) – Kess Energy, a leading junior lithium mining company, is pleased to announce that its Chairman, Inato Ramirez, has purchased 200,000 shares of Kess Energy, further demonstrating his confidence in the company’s future growth and its commitment to delivering value to stakeholders. Strengthening Leadership Commitment The purchase of 200,000 shares by Mr. Ramirez serves to reiterate his strong belief in Kess Energy’s strategic direction and the significant potential of its lithium projects. This investment aligns the Chairman’s interests with those of the company’s stakeholders and signals robust confidence in Kess Energy’s long-term prospects. Chairman’s Statement “I am excited about the future of Kess Energy and our role in driving the global transition to sustainable energy,” said Mr. Ramirez. “This personal investment reflects my full confidence in our team, our assets, and our ability to execute our growth strategy. I am committed to ensuring that we continue to deliver exceptional value to our stakeholders.” Company Vision and Growth Strategy Kess Energy is at the forefront of the lithium industry, focusing on sustainable mining practices and innovation in the South American “lithium triangle”. The company’s strategic initiatives include expanding its lithium production capacity, advancing exploration projects, and forging partnerships to support the burgeoning demand for lithium in electric vehicles and renewable energy storage. About Kess Energy Kess Energy is a junior lithium mining company dedicated to meeting the increasing global demand for lithium through responsible and sustainable mining practices that respect and consider the needs of the communities in which its assets are located. With a portfolio of high-quality lithium assets and a commitment to innovation, Kess Energy is well-positioned to play a pivotal role in the energy transition while enabling communities to share in the commercial benefits of its business.. Forward-Looking Statements This press release contains forward-looking statements that involve risks and uncertainties. These statements are based on current expectations and projections about future events and are not guarantees of future performance. Actual results may differ materially from those expressed or implied in these statements due to various factors. Know more please contact Phone No.: +55 61 4042 9257, or visit our office at: Centro Empresarial Varig SCN QUADRA 04 BL B – Asa Norte, Brasília – DF, 70714-900, Brazil. Media Contact Brand: Kess Energy Contact: Joseph Hera Email: contact@kessenergy.com Website: https://kessenergy.com The article is provided by a third-party content provider. SeaPRwire ( https://www.seaprwire.com/ ) makes no warranties or representations in connection therewith. Sectors: Top Story, Corporate News SeaPRwire provides real time press release distribution for companies and organizations to 6,500+ media outlets & 3.5 million professional desktops in 90 regions. It distributes press releases in different languages, including: IndonesiaFolk, IndoNewswire, SEATribune, IDNewsZone, LiveBerita, DailyBerita, TaiwanPR, SinchewBusiness, AsiaEase, BuzzHongKong, SingapuraNow, TIHongKong, TaipeiCool, TWZip, AsiaFeatured, dePresseNow, THNewson, KULPR, VNFeatured, MENAEntry, HunaTimes, DubaiLite, ArabicDir, BeritaDaring, TekanAsia, JamKopi ...
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Dr.Friend Puppy, Exhibits at Global Pet Show, Targeting Overseas Markets

Dr.Friend Puppy, Exhibits at Global Pet Show, Targeting Overseas Markets

Seoul, Korea – August 14, 2024 – (SeaPRwire) -The premium sleep and healthcare brand Dr.Friend’s pet sleep care product, Dr.Friend Puppy (owned by World Home Doctor Corp.), will be actively targeting overseas markets from the second half of the year. Dr.Friend Puppy will participate in the SUPER ZOO in Las Vegas, USA from August 14-16 to actively promote Dr.Friend’s unique sleep & healthcare technology. SUPER ZOO is one of the most established and prestigious pet industry trade shows in North America. It has been held since 1950, and it is considered the largest pet industry show in North America. It continues to be one of the most productive and vibrant shows yearly. Following CES2024 in January and IHS2024 in March, Dr.Friend Puppy will participate in Super Zoo to introduce its unique pet sleep care technology and pet humanization philosophy to pet industry stakeholders around the world. In particular, Dr.Friend Puppy is a pet-specific sleep care product that incorporates Dr.Friend’s sleep care technology, such as grounding technology and natural material technology. This has the advantage of harmonizing the natural characteristics of pets that are healthiest when they are in nature with the characteristics of their living environment. Dr.Friend’s core natural functional material technologies, such as charcoal wool with antibacterial properties and natural wool, are optimally proportioned to enhance pet sleep care without using chemicals such as memory foam, so pets can feel comfortable and stable sleeping environments every day. In addition, a water-repellent technology that coats a thin film on top of the fabric tissue is also applied to prevent contaminants that may occur due to the nature of the pet’s living environment from penetrating the surface of the fabric, making it more hygienic and convenient to use. By compensating for the disadvantage of sharing the same living environment as the owner, such as an apartment, pet grounding allows pets to get enough natural interaction in the comfort of their home. Dr.Friend will highlight various uniqueness and differentiation of Dr.Friend Puppy, such as realizing the value of pet humanization to ultimately maintain health, prevent various diseases, and reduce medical costs. “Dr.Friend’s grounding and natural material technology continues to gain scientific credibility through anti-inflammatory and stress relief studies that we have been conducting since 2018,” said Kim Ji Youn, CEO of Dr.Friend, who is participating in the exhibition. “In particular, the stress relief effect paper published in Biomedicines, an SCI-level journal, is showing high interest among animal healthcare professionals such as US veterinarians.” She also said, “As we are currently discussing clinical trials with domestic and foreign medical organizations to help improve pets’ health, we will actively promote the advantages of our sleep care technology and healthcare principles to expand cooperation opportunities with various buyers and partners.” After the Super Zoo exhibition, Dr.Friend Puppy will also participate in Pet Fair Asia, August 21-25 in Shanghai, China, expanding its growth strategy to the Asia Pacific region. Pet Fair Asia is Asia’s largest international pet products exhibition, and along with the Super Zoo, it is one of the world’s largest and most influential pet shows. This year’s event will be the largest since its inception in 1997, and Dr.Friend will present its authentic sleep &healthcare value and technology to more than 100,000 buyers and visitors, exploring opportunities to expand sales and establish strategic partnerships. About Dr. Friend Dr. Friend is a sleep care functional bedding brand that combines ergonomic functions and premium materials. It was created through continuous research and development for a long period of time to realize a safe and stable sleeping environment and to satisfy customers at all times. Media Contact Brand: Dr.Friend Puppy (World Home Doctor Corp.) Contact : Chon GyeongUn Email: cgu0823@worldhomedr.com Phone: +8210-4981-6360 Website: https://worldhome.global/ The article is provided by a third-party content provider. SeaPRwire ( https://www.seaprwire.com/ ) makes no warranties or representations in connection therewith. Sectors: Top Story, Corporate News SeaPRwire provides real time press release distribution for companies and organizations to 6,500+ media outlets & 3.5 million professional desktops in 90 regions. It distributes press releases in different languages, including: IndonesiaFolk, IndoNewswire, SEATribune, IDNewsZone, LiveBerita, DailyBerita, TaiwanPR, SinchewBusiness, AsiaEase, BuzzHongKong, SingapuraNow, TIHongKong, TaipeiCool, TWZip, AsiaFeatured, dePresseNow, THNewson, KULPR, VNFeatured, MENAEntry, HunaTimes, DubaiLite, ArabicDir, BeritaDaring, TekanAsia, JamKopi ...
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C14 Enters into Partnership with Tune.FM

C14 Enters into Partnership with Tune.FM

New York, NY – August 14, 2024 – (SeaPRwire) – C14, a leading provider of fiat-to-crypto on and off-ramp solutions, has joined forces with Tune.FM, a cutting-edge music NFT trading platform, to release an off-ramp solution for JAM, the native token of the Tune.fm application. This collaboration marks a significant step forward in the integration of cryptocurrency with the music industry, providing users with seamless conversion of JAM tokens to fiat currency. Tune.fm is a revolutionary platform where artists and fans can trade music NFTs, unlocking new revenue streams and interactive experiences in the music ecosystem. The native token, JAM, is at the heart of Tune.fm’s economy, facilitating transactions and rewarding artists and fans alike. With the introduction of an off-ramp solution, users will now have the ability to convert JAM tokens into fiat currency, enhancing the platform’s usability and accessibility. This partnership deepens C14 and Tune.fm’s existing relationship, where C14 provides on-ramping services for Tune.fm’s existing base of over TK users. C14 provides ramping services for JAM for users in over two dozen countries. JAM is built on the Hedera Hashgraph, a low cost, high throughput distributed ledger technology. C14 has established itself as a trusted partner in the crypto space, offering robust solutions that bridge the traditional financial system with the digital asset world. The off-ramp for JAM tokens leverages C14’s secure and efficient infrastructure, ensuring a smooth and reliable conversion process. C14 and Tune.FM will roll out service for users in the United States versus ACH first, with instant SEPA payouts to the European Union following soon after. Key Benefits of the Collaboration Seamless Conversion: Users can easily convert their JAM tokens into fiat currency, broadening the utility and acceptance of JAM in the real world. Enhanced Accessibility: The off-ramp solution lowers the barriers for new users to engage with Tune.FM, providing a straightforward method to cash out their JAM tokens. Security and Trust: C14’s proven track record in the industry ensures a safe and compliant process for all transactions, instilling confidence in users. “Partnering with Tune.fm aligns perfectly with our mission to make crypto accessible to everyone,” said Erich Grant, CEO of C14. “We are excited to support the vibrant community of artists and fans on Tune.fm by providing an easy and secure way to convert JAM tokens to fiat currency.” “This collaboration with C14 is a game-changer for our platform,” added Andrew Antar, CEO of Tune.FM. “The off-ramp solution not only enhances the user experience but also paves the way for wider adoption of JAM tokens in the mainstream economy.” The off-ramp for JAM tokens is expected to be available to Tune.FM users starting July 25th For more information on how to use the off-ramp, visit Tune.FM. About C14 C14 is a leading provider of fiat-to-crypto on and off-ramp solutions, dedicated to bridging the gap between traditional finance and the digital asset economy. With a focus on security, compliance, and user experience, C14 offers seamless conversion services that empower users to interact with the crypto world effortlessly. To know more please contact +1 (845) 366-6902. About Tune.FM Tune.fm is a pioneering music NFT trading platform that empowers artists and fans to engage in a vibrant digital music economy. By leveraging blockchain technology and the JAM token, Tune.FM enables transparent and rewarding interactions within the music industry, fostering a new era of music ownership and distribution. Media Contacts Erich Grant, Founder of C14 erich@c14.money Website: https://c14.money/ Andrew Antar, Founder of Tune.FM hello@Tune.FM Website: http://tune.fm/ The article is provided by a third-party content provider. SeaPRwire ( https://www.seaprwire.com/ ) makes no warranties or representations in connection therewith. Sectors: Top Story, Corporate News SeaPRwire provides real time press release distribution for companies and organizations to 6,500+ media outlets & 3.5 million professional desktops in 90 regions. It distributes press releases in different languages, including: IndonesiaFolk, IndoNewswire, SEATribune, IDNewsZone, LiveBerita, DailyBerita, TaiwanPR, SinchewBusiness, AsiaEase, BuzzHongKong, SingapuraNow, TIHongKong, TaipeiCool, TWZip, AsiaFeatured, dePresseNow, THNewson, KULPR, VNFeatured, MENAEntry, HunaTimes, DubaiLite, ArabicDir, BeritaDaring, TekanAsia, JamKopi ...
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