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Milestone reinforces leadership in AI-powered breast cancer detection WELLINGTON, New Zealand, Oct. 25, 2024 /PRNewswire/ -- Volpara Health, a Lunit company and global leader in artificial intelligence (AI)-powered breast health solutions, has reached a significant milestone: the publication of the 300th peer-reviewed scientific paper using Volpara results. This accomplishment underscores Volpara's commitment to advancing breast cancer detection and personalized care through evidence-based AI technologies. The need for robust, peer-reviewed validation in mammography AI is essential to its clinical adoption. A review of 100 CE-marked AI products in radiology revealed that 64% lacked peer-reviewed evidence of efficacy. Volpara, in contrast, leads the mammography AI industry with the most peer-reviewed scientific papers, demonstrating its innovative technologies are rigorously tested, and clinically validated. "Reaching 300 studies reflects the deep trust our technology has earned within both the academic and clinical communities," said Teri Thomas, CEO of Volpara Health and CBO of Lunit. "Our commitment to peer validation provides important evidence of our AI solutions' ability to deliver measurable improvements in detection and patient outcomes." Two recent studies showcase the benefits of Volpara's AI technology. Breast density-based mammogram ordering enhances interpretation Enhancing Radiologist Reading Performance by Ordering Screening Mammograms Based on Characteristics That Promote Visual Adaptation, shows how ordering mammograms based on breast density can improve radiologists' performance. By arranging mammograms from low to high volumetric breast density (VBD), radiologists reduced reading time and increased specificity from 86% to 89%, leading to greater accuracy in detecting cancer. Commenting in an editorial on the study, Dr. Lars Grimm explained, "Deliberate ordering of screening mammograms could be introduced into workflows very easily because it dovetails with existing batch-reading strategies." Study confirms Volpara's AI identifies Women at higher risk for missed cancers Breast Density Effect on the Sensitivity of Digital Screening Mammography in a UK Cohort, used Volpara's AI-powered algorithms to determine how breast density affects cancer detection in the UK. The study confirmed that Volpara's technology effectively identifies women at higher risk for missed cancers on mammography, reinforcing the importance of personalized screening strategies. Melissa Hill, PhD, Senior Imaging Scientist and Global Research Lead at Volpara Health, emphasized the significance of scientific rigor: "Our research collaborations and commitment to innovation have brought us to this important milestone. Each published paper puts our technology to the test, and robust results strengthen the trust clinicians place in Volpara to help improve patient care." The company's journey from its first to its 300th peer-reviewed paper reflects over 15 years of innovation and investment in research. Volpara remains committed to pushing the boundaries of AI to improve breast health. For more information about Volpara Health and new research to be presented at RSNA 2024, visit volparahealth.com/rsna2024. About Volpara Health Volpara Health is on a mission to save families from cancer with AI-powered software that helps healthcare providers better understand cancer risk, guide personalized care decisions, and recommend additional imaging and interventions. Used in over 3,500 facilities by more than 5,600 technologists worldwide. Volpara's software impacts nearly 18M patients, supports over 3.6M annual cancer risk assessments, and integrates seamlessly with electronic health records and imaging systems. Volpara helps radiologists quantify dense breast tissue with precision and technologists produce mammograms with optimal positioning, compression, and dose. Volpara software also streamlines operations to ease compliance and accreditation. Volpara, a Lunit company, is headquartered in Wellington, New Zealand, and has an office in Seattle. Volpara is the trusted partner of leading healthcare institutions globally. For more information, visit www.volparahealth.com. Logo - https://mma.prnasia.com/media2/389465/Volpara_Health_Logo.jpg?p=medium600
- The first tri-party executive roundtable was held in London to strengthen synergies for Seegene's vision of creating 'a world free from diseases' - Preliminary results of product development automation and statistical analysis of syndromic test results powered with Microsoft's AI technology were showcased - Global experts and scientists participated in building a diagnostic product development eco-system utilizing Springer Nature's scientific network - Companies fostered collaboration to drive collective impact towards next year's 'a world free from diseases' declaration ceremony SEOUL, South Korea, Oct. 24, 2024 /PRNewswire/ -- Seegene Inc., a leading South Korean company providing a total solution for PCR molecular diagnostics, held the first executive roundtable with Microsoft and Springer Nature to discuss advancing its technology-sharing initiative aimed at mitigating future pandemics and creating 'a world free from diseases', including the showcase of preliminary results from an automated diagnostic development system powered with Microsoft's artificial intelligence (AI) technology. This is the first official event that the three companies gathered to discuss the initiative. [Photo 1] ▲ From left: Marc Spenlé, COO of Springer Nature; Dr. Jong-Yoon Chun, CEO and Founder of Seegene; and Elena Bonfiglioli, Vice President of Global Business Leader Healthcare, Pharma and Life Science at Microsoft posed for a photo during Technology-Sharing Initiative Partner Roundtable in Springer Nature Campus, London, United Kingdom on October 23, 2024. On October 23, the three companies convened at Springer Nature London Campus Auditorium for the technology-sharing initiative partner roundtable to share initial achievements and explore strategies for further collaboration. Dr. Jong-Yoon Chun, CEO and founder of Seegene; Marc Spenlé, chief operating officer of Springer Nature; Steven Inchcoombe, president of research at Springer Nature; and Elena Bonfiglioli, vice president of global business leader healthcare, pharma and life science at Microsoft attended the meeting. "By integrating Seegene's proprietary syndromic real-time PCR technology, Microsoft's cutting-edge AI and cloud services, and Springer Nature's extensive reach in the global scientific community, we will create new avenues for collaboration with scientists and experts in this technology-sharing initiative," said Dr. Chun, CEO and founder of Seegene. The technology-sharing initiative aims to globally share Seegene's advanced diagnostic and data analysis technologies, including syndromic real-time PCR and an automated product development system (SGDDS), with a leading company partnered in each country. Partnering companies will collaborate with local scientists and experts to develop diagnostic tests tailored to the needs of their communities and fields, spanning a wide range of human and non-human diseases. Amidst the challenges of climate change and the anticipated rise in outbreaks, the initiative's ultimate vision is to create 'a world free from diseases'—a future where people no longer suffer from infectious diseases and cancer, and where animals and plants thrive without illness. Seegene's syndromic real-time PCR technology represents a breakthrough in molecular target detection, unparalleled by other PCR methods. It enables the simultaneous detection of up to 14 pathogens in a single reaction tube, with quantitative information for each target. Furthermore, multi-tube panel tests may be designed to cover an even more comprehensive set of pathogens with overlapping symptoms. As a powerful tool for mitigating the growing threat of multi-pandemics—exacerbated by climate change—Seegene's technology enhances the ability to monitor and respond to a diverse range of rapidly evolving pathogens. Companies participating in the technology-sharing initiative will gain access to Seegene's cutting-edge technology and expertise, enabling them to develop and manufacture syndromic real-time PCR products tailored to their countries' specific public health needs. Localization of such capabilities through this initiative will allow their communities to promptly respond to future outbreaks and multi-pathogen pandemics. Building on the momentum achieved during this year's roundtable, a declaration ceremony is expected to take place in the second half of next year, where strategies to maximize synergy amongst the three company's technology will be further discussed. At the meeting in London, Seegene and Microsoft showcased the preliminary results of integrating Microsoft's Azure Open AI into the research planning module of Seegene's automated product development system (SGDDS). The use of AI technology dramatically reduced the time needed to process and analyze relevant information from published scientific literature. Additionally, the two companies demonstrated a proof of concept for Seegene's syndromic-based statistical analysis system that leverages Fabric, Microsoft's AI-driven data integration platform, ultimately to discover statistical correlations between multiple pathogens causing similar symptoms, support accurate diagnosis and treatment, and predict future outbreaks. "Until now, scientists and experts have been confined to limited local data, usually generated by themselves. However, access to diagnostic information shared across the world powered with Microsoft's AI technology will enable swift response to any emerging diseases," said Dr. Chun at Seegene. "Seegene and Microsoft shared the vision of a new generation of diagnostic solutions, accessible at population level to help people stay healthier longer. Cloud and AI solutions help protect, manage and reason over the vast amounts of data needed to track diagnosis of global diseases in real time. Microsoft is the trusted partner to help realize Seegene's vision of building 'a world free from diseases,'" said Ms. Bonfiglioli from Microsoft. In January 2024, Seegene and Microsoft entered a strategic collaboration to integrate Microsoft's Azure Open AI services into numerous modules of Seegene's SGDDS. The goal of these collaborative projects is to empower global companies participating in the technology-sharing initiative with a streamlined product development system augmented by advanced IT system operations and AI-powered data analysis. Springer Nature was also present at the discussion. Since 2023, Seegene and Springer Nature have been running the Open Innovation Program (OIP) that invited scientists and experts around the world to participate in the development of clinically significant diagnostics assays. This year, the program was renewed by Springer Nature as the prestigious Nature Awards, MDx Impact Grants, calling for innovative proposals for PCR diagnostic assay development. Springer Nature will oversee key aspects of the process, including project submissions and evaluations, expecting to broaden interest and participation from the global scientific community. In May 2024, the two companies signed a strategic alliance agreement that included expansion of the OIP program scope. Springer Nature will encourage the global scientific community to participate in the ideation, design, and development of new PCR diagnostic products. "We have high expectations that the MDx Impact Grants will work synergistically with the technology-sharing initiative serving as a catalyst for greater adoption of PCR molecular diagnostics. Together we will build an ecosystem that promotes the development of accurate, rapid, accessible tests for underserved patient populations." said Mr. Spenlé, the COO of Springer Nature. An OIP Award ceremony was held, following the technology-sharing initiative partner roundtable to recognize the European winners. At the ceremony, eight scientists working in Europe among 17 awardees across the world were honored for their achievements. The awardees were as follows: Ulrich Eigner (Germany); Gian Maria Rossolini (Italy); Vismara Chiara Silvia (Italy); Davy Vanden Broeck (Belgium); Nicolas Yin (Belgium); Piet Cools (Belgium); Khoa Thai (Netherlands); Pedro Vieira-Baptista (Portugal). Prof. Dame Jenny Harries, Chief Executive of the UK Health Security Agency (UKHSA), attended the event as a keynote speaker. During her visit to South Korea in March this year, Prof. Harries met with Dr. Chun at Seegene's headquarters to discuss Seegene's response and achievements during the COVID-19 pandemic, as well as to exchange views on its technology-sharing initiatives and the Open Innovation Program (OIP). Companies participating in the technology-sharing initiative, such as Hy Laboratories Ltd. based in Israel and Werfen based in Spain, along with other business partners and bio-medical experts from Europe, attended the event to share the vision of the technology-sharing initiative. About Seegene Seegene has 24 years of dedicated experience in R&D, manufacturing, and business related to syndromic real-time PCR technologies. This expertise was particularly highlighted during the COVID-19 pandemic when Seegene provided over 340 million COVID-19 tests to more than 100 countries worldwide. The core feature of Seegene's syndromic real-time PCR technology is the ability to simultaneously test for 14 pathogens that cause similar symptoms in a single tube with quantitative information. Visit: Seegene.com and follow linkedin.com/company/seegene-inc [Photo 2] ▲ From Right: Dr. Jong-Yoon Chun, CEO and Founder of Seegene; Professor Dame Jenny Harries, Chief Executive of the UK Health Security Agency; Elena Bonfiglioli, Vice President of Global Business Leader Healthcare, Pharma and Life Science at Microsoft; and Marc Spenlé, COO of Springer Nature posed for a photo during Open Innovation Award ceremony in Springer Nature Campus, London, United Kingdom on October 23, 2024.
IVD leader adopts MasterControl Qx and Mx platforms to ensure regulatory compliance across China, the US and more. SINGAPORE, Oct. 23, 2024 /PRNewswire/ -- MasterControl announced today that CorDx Inc., the global diagnostics company and leader in IVD research and development, has chosen MasterControl Qx and Mx to help enhance quality management and manufacturing processes across its business. With MasterControl's best-in-class automation and machine learning tools, CorDx Inc. will bring diagnostic tests and capabilities to clients faster and more efficiently so patients can better monitor and improve their overall health. "Because regulations differ across international borders, it's critical that we have a solution that helps us understand, manage and remain compliant with those standards, regardless of whether we are operating in the US, China or elsewhere," said Aiiso Yufeng Li, CorDX Inc. Founder and Chief Strategy Officer. "MasterControl provides the global capability that ensures we can work seamlessly without having to worry about slip ups in our quality control or manufacturing operations. It allows us to keep our focus on bringing innovations to the people and families that need it most." MasterControl's Qx and Mx offerings give customers no-code options to customize, build and optimize quality event forms and workflows, rapidly digitize manufacturing processes and procedures, and automate training management. The platforms integrate across operating systems like ERPs, IoT devices, LIMS and more to provide seamless data connectivity, real-time status updates, and automated workflows. "CorDx Inc. leads the industry in IVD research and development and is pushing the boundaries on diagnostics," said Sue Marchant, chief product officer at MasterControl. "Removing regulatory hurdles and operational inefficiencies from workflows will not only improve overall performance, but it will also give CorDx Inc. the freedom to innovate and make new and meaningful impact in the lives of people across the world." To learn how more than 1,100 MasterControl customers are bringing life-changing products to market faster and for less, visit: https://www.mastercontrol.com/company/customers/. About MasterControl:MasterControl Inc. is a leading provider of cloud-based software solutions that enable regulated companies to deliver life-changing products to more people sooner. MasterControl's manufacturing and quality management software solutions help organizations innovate faster, reduce costs, and improve compliance by automating and securely managing critical business processes throughout the entire product life cycle. For more information, visit www.mastercontrol.com. About CorDx: With nearly two decades of IVD experience, CorDx Inc is a leader in IVD research and development, manufacturing, and supply chain. CorDx Inc.'s proprietary line of rapid diagnostic products is recognized by families, medical professionals & veterinarians for reliability, affordability, and rapid results. CorDx is transforming the global diagnostics industry with innovative R&D solutions, a vertically integrated supply chain, and manufacturing footprints in China, United States and around the world.
Two new studies show Lunit INSIGHT MMG cuts radiologist workload by 50% in a double reading environment while maintaining or improving screening quality, and predicts cancer risk up to six years in advance SEOUL, South Korea, Oct. 23, 2024 /PRNewswire/ -- Amid rising demands and a global shortage of radiologists, Lunit (KRX:328130.KQ), a leading provider of AI-powered solutions for cancer diagnostics and therapeutics, today announced pivotal findings from two large-scale studies evaluating its AI-powered mammography solution, Lunit INSIGHT MMG. The studies conducted by researchers at the Cancer Registry of Norway and Odense University Hospital in Denmark demonstrate the technology's potential to significantly improve breast cancer screening programs. Lunit INSIGHT MMG, Lunit's AI-powered mammography analysis solution, showcased its ability to predict breast cancer risk and assist in streamlining radiologist workflows. The Norwegian study, published in JAMA Network Open, led by Professor Solveig Hofvind, evaluated how Lunit INSIGHT MMG could estimate the development of future cancer. The research analyzed data from 116,495 women aged 50-69 who underwent at least three consecutive biennial screening rounds at 9 breast centers in Norway. The research found that Lunit INSIGHT MMG can estimate future breast cancer risk up to 4 to 6 years before it becomes detectable. Lunit's AI assigns each breast a score from 0 to 100, with higher values indicating a greater likelihood of cancer being present on the current mammogram. The study found that the mean AI scores were consistently higher for breasts that developed cancer compared to those that remained cancer-free, even 4 to 6 years before detection. Over multiple screening rounds, the gap in these AI scores between breasts that developed cancer and those that did not grew larger, indicating the AI's ability to detect subtle signs of cancer earlier. Specifically, for women who developed screen-detected cancer, the mean absolute differences in AI scores between the two breasts were 21.3 in the first study round, 30.7 in the second, and 79.0 in the third. Additionally, Lunit's AI achieved an Area Under the Curve (AUC) for the absolute difference of 0.63, 0.72, and 0.96 across the three screening rounds for screen-detected cancer. These findings indicate that Lunit's AI can effectively identify early signs of cancer and offer a pathway for personalized screening approaches. The double reading of mammograms, though the standard of care in Denmark and other European regions, is resource-intensive and demands significant radiologist time. The Danish study, led by Dr. Mohammad T. Elhakim and published in Radiology: Artificial Intelligence, explored how Lunit INSIGHT MMG could enhance double reading without compromising screening performance. The research team evaluated three AI-integrated screening scenarios on 249,402 mammograms, demonstrating significant reductions in radiologist workload while either maintaining or improving accuracy (Scenario 1: AI replaced first reader; Scenario 2: AI replaced second reader; Scenario 3: AI replaced both for triaging of low and high-risk cases). Results showed that replacing the first, second, or both radiologists with Lunit's AI could reduce reading volume by 48.8%, 48.7%, and 49.7%, respectively, while maintaining or improving cancer detection accuracy. Most notably, the AI triage scenario (Scenario 3) achieved higher sensitivity, positive and negative predictive values with a lower arbitration rate when compared to standard double reading. This result highlights that by utilizing Lunit INSIGHT MMG, healthcare systems can significantly reduce radiologists' burden without compromising the screening program's diagnostic performance quality, allowing them to focus on more complex cases and improving overall efficiency. "These studies provide compelling evidence of our AI's potential to transform breast cancer screening," said Brandon Suh, CEO of Lunit. "In Norway, our AI identified future breast cancer risk up to 6 years ahead, providing women and healthcare providers valuable time for proactive interventions. The Danish study showed a 50% reduction in radiologist workload without sacrificing detection quality—a result that directly impacts radiology efficiency worldwide. These are not hypothetical improvements; they represent concrete benefits that healthcare providers and patients are experiencing today. Our focus is on ensuring these advancements translate directly to better outcomes for women undergoing breast cancer screening." About Lunit Founded in 2013, Lunit (KRX:328130.KQ) is a medical AI company on a mission to conquer cancer. We harness AI-powered medical image analytics and AI biomarkers to ensure accurate diagnosis and optimal treatment for each cancer patient. Our FDA-cleared Lunit INSIGHT suite for cancer screening serves over 3,500 hospitals and medical institutions across 50+ countries. Our clinical studies have been published in top journals, including the Journal of Clinical Oncology and the Lancet Digital Health, and presented at global conferences such as the ASCO and RSNA. In 2024, Lunit acquired Volpara Health Technologies, setting the stage for unparalleled synergy and accuracy, particularly in breast health and screening technologies. Headquartered in Seoul, South Korea, with a network of offices worldwide, Lunit leads the global fight against cancer. Discover more at lunit.io.
BEIJING, Oct. 21, 2024 /PRNewswire/ -- Datasea Inc. (NASDAQ: DTSS) ("Datasea" or the "Company"), a Nevada-based digital technology company focused on innovative high-tech acoustics and 5G AI multimodal digital technology, today announced that, as of October 15, 2024, the Company closed its Regulation S offering (the "Offering") with three investors, including its two largest shareholders, the Company's CEO and Director, pursuant to which the Company sold the investors an aggregate of 1,932,224 shares of its common stock (the "Shares"). The purchase price for the Shares was $2.06 per share, which was equal to the closing price of the Company's common stock on The Nasdaq Capital Market on September 26, 2024, the date on which the binding subscription agreements had been entered into by the parties. The investors have agreed to hold the shares for a period of no less than 180 days. The investors in the Offering include two members of the Company's management, who are also major shareholders, reflecting their strong confidence in the Company's future development. The funds raised, in the amount of approximately $4.0 million, will primarily be used to support the Company's future business operations, including investments in acoustic high-tech related products design upgrade, working capital for mass production and on-line sales, acquiring intellectual property and working capital for the promotion and sales of 5G AI multimodal digital business products. Ms. Zhixin Liu, CEO of Datasea stated, "We are pleased to receive support from our major shareholders, which not only enhances market confidence in our development but will also help us accelerate the achievement of our strategic goals." About Datasea Inc. Datasea is a leading provider of products, services, and solutions for enterprise and retail customers in two innovative industries, acoustic high tech and 5G-AI multimodal digitalization. The Company's advanced R&D technology serves as the core infrastructure and backbone for its products. Its 5G multimodal communication segment operates on a cloud platform based on AI. Datasea leverages cutting-edge technologies, precision manufacturing and ultrasonic, infrasound and directional sound technology in its acoustics business to combat viruses and prevent human infections, and it is also developing applications in medical ultrasonic cosmetology. In July 2023, Datasea established a wholly-owned subsidiary, Datasea Acoustics LLC, in Delaware, in a strategic move to enter the U.S. markets and to mark its global expansion plan. For additional information, please visit www.dataseainc.com. Cautionary Note Regarding Forward-Looking Statements This press release contains forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934 and as defined in the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements can be identified by terminology such as "will", "expects", "anticipates", "future", "intends", "plans", "believes", "estimates", "target", "going forward", "outlook," "objective" and similar terms. Such statements are based upon management's current expectations and current market and operating conditions, and relate to events that involve known or unknown risks, uncertainties and other factors, all of which are difficult to predict and which are beyond Datasea's control, which may cause Datasea's actual results, performance or achievements (including the RMB/USD value of its anticipated benefit to Datasea as described herein) to differ materially and in an adverse manner from anticipated results contained or implied in the forward-looking statements. Further information regarding these and other risks, uncertainties or factors is included in Datasea's filings with the SEC, which are available at www.sec.gov. Datasea does not undertake any obligation to update any forward-looking statement as a result of new information, future events or otherwise, except as required under law. Investor and Media Contact: Datasea Investor RelationsEmail: investorrelations@shuhaixinxi.com sunhezhi@shuhaixinxi.com
HAMBURG, Germany, Oct. 21, 2024 /PRNewswire/ -- Mediso is unveiling its new AnyScan® TRIO SPECT/CT, TheraMAX* scanner at the annual meeting of European Association of Nuclear Medicine (EANM). The first global installation of the AnyScan TRIO SPECT/CT, TheraMAX at University Hospital Regensburg The new TheraMAX is specifically designed for serving the clinical needs of theranostic imaging. It features detectors and collimators developed for Targeted Radionuclide Therapies carried out with radioisotopes emitting not only alpha and beta particles, but high and ultra-high energy gamma photons like 177Lu, 212Pb, 131I, 225Ac and beyond. The TheraMAX is equipped with three, large surface detectors (up to 5x larger than 12-detector CZT systems) surrounding the patients completely (360°). The 15.9mm thick NaI crystals ensure improved sensitivity for high energy photons, while the high-density sensor arrangement (123 PMT per detector head) allows high spatial resolution leading to PET-like image quality in all NM applications. The 300% sensitivity gain compared to conventional dual-detector systems enables whole body 225Ac SPECT/CT in theranostic imaging, while this extreme total system response also allowing ultra-fast quantitative total-body SPECT/CT scans with 99mTc and LEHR-HS collimator. Moreover, novel multi-pinhole technology combined with Triple-NaI-Detectors provide outstanding performance for cardiology and neurology. The integrated CT offers three performance levels: low-dose diagnostic scans, ultra-low dose protocol for attenuation and scatter correction and even "Zero-Dose" imaging with AI-powered SyCT** (Synthetic CT). The first global site for the TheraMAX is the University Hospital Regensburg, Germany. Following a recent installation, Professor Dr. Dirk Hellwig, the head of the Department of Nuclear Medicine said "the new scanner will boost our diagnostic and theranostic workflow, leading to better patient care and it also opens new possibilities in clinical research". "With the development of the new TheraMAX, we extended the imaging capabilities of nuclear medicine departments by improving the diagnostic confidence of SPECT/CT examinations close to PET/CT" said Istvan Bagaméry, Managing Director of Mediso Ltd. "The TheraMAX transforms the clinical routine also with ultra-fast quantitative total-body scans." About Mediso Mediso is a leading manufacturer of molecular imaging techniques to the health care and medical research institutions of the world. Mediso has a complete profile of imaging research, system development, manufacturing, selling and servicing of multi-modality imaging devices. With over 35-years of expertise, 1400 clinical and 350 preclinical systems installed in over 100 countries, Mediso offers complete solutions from imaging devices to evaluation and quantification software. *TheraMAX is the configuration name of AnyScan TRIO SPECT/CT with MAX/123-15.9 detector **Regulatory approval pending Contact: info@mediso.comhttps://mediso.com/ Photo - https://mma.prnasia.com/media2/2526761/Mediso.jpg?p=medium600Logo - https://mma.prnasia.com/media2/2526762/Mediso_Logo.jpg?p=medium600
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