SHENZHEN, Feb 24, 2026 - (ACN Newswire via SeaPRwire.com) - China Medical System Holdings Limited (“CMS” or the “Group”) is pleased to announce that its subsidiary, Dermavon Holdings Limited (“Dermavon”, an innovative pharmaceutical company specialized in skin health which is applying for a separate listing on the Main Board of The Stock Exchange of Hong Kong Limited, please refer to the announcement published by the Group on 22 April 2025 for details) received the acceptance from the National Medical Products Administration of China (NMPA) for the New Drug Application (NDA) of ruxolitinib phosphate cream (the “Product”) for the treatment of mild to moderate atopic dermatitis on 24 February 2026. The Product is indicated for the topical short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis in non-immunocompromised adult and pediatric patients 2 years of age and older whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable. The NDA has been approved for inclusion in the Priority Review List by the Center for Drug Evaluation (CDE) of the NMPA based on its qualification as a “new variety, dosage form and specification of pediatric drug that conforms to the physiological characteristics of children”, which is expected to accelerate the Product's review process for marketing approval in the AD indication.Impressive phase III trial data in ADIts Priority Review is expected to accelerate its NDA approvalRuxolitinib phosphate cream was approved for marketing by the NMPA in January 2026, becoming the first and only targeted drug approved in China for the treatment of vitiligo. The acceptance of this NDA for the additional indication of AD marks a key milestone in the Product's expansion into multiple therapeutic areas.Ruxolitinib phosphate cream has achieved positive results in a randomized, double-blind, placebo-controlled Phase III clinical trial in China for mild to moderate AD.Robust Efficacy: The Product successfully met its primary endpoint, demonstrating that a significantly higher proportion of subjects treated with ruxolitinib phosphate cream achieved IGA (Investigator’s Global Assessment) of 0 or 1 with at least two grades of reduction from baseline at week 8, compared with placebo (63.0% vs 9.2%, P < 0.001). For the key secondary endpoint, the proportion of subjects achieving at least a 75% improvement from baseline in the Eczema Area and Severity Index score (EASI 75) of treatment with ruxolitinib phosphate cream was also significantly higher than that of the placebo group, at week 8 (78.0% vs 15.4%, P < 0.001).Favorable Safety Profile: The severity of treatment-emergent adverse events (TEAE) during the treatment period was mostly mild or moderate, with no TEAEs leading to discontinuation of the study drug. Overall, ruxolitinib phosphate cream was safe and well-tolerated.Furthermore, the NDA has been approved for inclusion in the Priority Review List. According to relevant NMPA regulations, the review timeline for marketing applications subject to Priority Review and Approval Procedure is substantially shortened—from the standard 200 days to 130 days. This significant reduction in the review timeline is expected to accelerate the marketing process of ruxolitinib phosphate cream for the AD indication, benefiting a wide range of patients at an earlier date.Building an integrated AD solution,strengthening Dermavon’s leadership in dermatologyAD is a chronic, recurrent and inflammatory dermatologic disease, with the main clinical manifestations of dry skin, chronic eczema-like lesions and obvious itching or pruritus, which may seriously affect the quality of life of patients. It is estimated that there were over 54 million AD patients in China as of 2024. Based on SCORAD scores, mild to moderate AD accounts for 98% of these cases, representing over 52.5 million patients[1]. Topical drugs are the most basic treatment for AD. Traditional topical medications such as topical corticosteroids (TCS) and topical calcineurin inhibitors (TCIs) have clinical pain points with long-term adverse reactions or limited efficacy, therefore novel treatments are urgently needed.Dermavon has developed a comprehensive “treatment + care” integrated solution for AD. In addition to the topical formulation ruxolitinib phosphate cream for mild-to-moderate AD, the portfolio also includes the injectable biological agent Comekibart Injection (MG-K10) for moderate-to-severe AD, the oral small molecule targeted drug CMS-D001 for moderate-to-severe AD, and the Heling Soothing Product Series for daily repair, to meet the management needs of AD patients from treatment to daily care.Simultaneously, the acceptance of the NDA for the AD indication will strengthen Dermavon’s strategic layout in the field of skin treatments and create synergies with its commercialized innovative drug ILUMETRI (tildrakizumab injection), commercialized exclusive drug Hirudoid (mucopolysaccharide polysulfate cream), and a series of innovative drugs under development and dermatological skin care products, in terms of expert network and market resources, thereby potentially enhancing Dermavon's market competitiveness and brand influence in the field of skin health.More Information About Ruxolitinib Phosphate CreamRuxolitinib phosphate cream (Opzelura®), a novel cream formulation of the selective JAK1/JAK2 inhibitor ruxolitinib developed by Incyte. In China, ruxolitinib phosphate cream is approved for the treatment of non-segmental vitiligo with facial involvement in children aged 12 years and older and adult patients. In the U.S., ruxolitinib phosphate cream is the first topical JAK inhibitor approved by the U.S. Food and Drug Administration (FDA) for the topical treatment of non-segmental vitiligo in patients aged 12 years and older, and for the topical short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis in non-immunocompromised adult and pediatric patients 2 years of age and older whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable[2]. In Europe, ruxolitinib phosphate cream is approved for the treatment of non-segmental vitiligo with facial involvement in adults and adolescents from 12 years of age[3].The Group, through its subsidiary of Dermavon entered into a Collaboration and License Agreement with Incyte for ruxolitinib phosphate cream on 2 December 2022, obtaining an exclusive license to develop, register and commercialize the Product in Mainland China, Hong Kong Special Administrative Region, Macau Special Administrative Region, Taiwan Region and eleven Southeast Asian countries (the “Territory”) and a non-exclusive license to manufacture the Product in the Territory. The subsidiary of Dermavon has sublicensed the relevant rights for the Product outside of Mainland China to the Group (excluding Dermavon and its subsidiary).Incyte has worldwide rights for the development and commercialization of ruxolitinib phosphate cream, marketed in the United States and Europe as Opzelura®. Opzelura® and the Opzelura® logo are registered trademarks of Incyte.About CMSCMS 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 in its advantageous specialty fields, strengthening the competitiveness of the cardio-cerebrovascular/ gastroenterology/ ophthalmology/ skin health businesses, bringing economies of scale in specialty fields. Among them, the skin health business (Dermavon) has become a leading enterprise in its field, and is proposed to be listed independently on the SEHK. Meanwhile, CMS continuously promotes the operation and development of its integrated R&D, manufacturing and commercialization chain in Southeast Asia and the Middle East, capturing growth opportunities in emerging markets to support the high-quality and sustainable development of the Group.Reference:1. China Insights Consultancy’s industrial report2. The U.S. FDA approval information can be found on the Incyte official website, as follows:https://investor.incyte.com/news-releases/news-release-details/incyte-announces-additional-fda-approval-opzelurar-ruxolitinib3. The EMA approval information can be found on the Incyte official website, as follows:https://investor.incyte.com/news-releases/news-release-details/incyte-announces-european-commission-approval-opzelurarCMS Disclaimer and Forward-Looking StatementsThis 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 ContactBrand: China Medical System Holdings Ltd.Contact: CMS Investor RelationsEmail: ir@cms.net.cnWebsite: https://web.cms.net.cn/en/home/ Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

深圳, 2026年2月24日 - (亚太商讯 via SeaPRwire.com) - 康哲药业控股有限公司 （"康哲药业"）欣然宣布，旗下德镁医药有限公司（"德镁医药"，专业聚焦皮肤健康的创新型医药企业，正申请于香港联合交易所有限公司主板独立上市，详见康哲药业日期为2025年4月22日发布的公告）已于2026年2月24日获得中国国家药品监督管理局（NMPA）受理磷酸芦可替尼乳膏（"产品"）轻中度特应性皮炎（"AD"）的新药上市许可申请（NDA）。产品拟用于其他外用药控制不佳或不建议使用时，非免疫功能受损的2岁及以上儿童和成人轻中度特应性皮炎的局部短期和非持续性慢性治疗。且该项NDA因"符合儿童生理特征的儿童用药品新品种、剂型和规格"，已获得NMPA药品审评中心批准纳入优先审评品种名单，有望加快产品AD适应症上市审评进程。特应性皮炎III期临床数据亮眼，优先审评加速上市磷酸芦可替尼乳膏已于2026年1月获得NMPA批准上市，成为中国批准的首款且唯一用于白癜风治疗的靶向药。此次增加AD适应症NDA获受理，是产品向多治疗领域拓展的关键里程碑。磷酸芦可替尼乳膏已在轻中度AD的一项随机、双盲、安慰剂对照中国三期药物临床研究取得积极结果：- 疗效优异：产品成功达到主要终点，即使用产品治疗8周，达到研究者整体评估（IGA）评分为0或1分，且较基线改善≥2分的受试者比例，显著高于安慰剂（63.0% vs 9.2%，P

HONG KONG, Feb 24, 2026 - (ACN Newswire via SeaPRwire.com) – CanSino Biologics Inc. (688185.SH/06185.HK) announced that the Company has obtained the Notification of Approval of Supplemental Drug Application issued by the National Medical Products Administration of China (the “NMPA”), pursuant to which, the supplemental application to expand the age range of applicable population of the Company’s Group ACYW135 Meningococcal Polysaccharide Conjugate Vaccine (CRM197) (the “MCV4”, trade name: Menhycia (R)) from “children aged from 3 months to 3 years old (47 months)” to “children aged from 3 months to 6 years old (83 months)” has been approved by NMPA.This approval marks an important step forward, underscoring the public health impact of Menhycia (R) while also strengthening its long-term commercial prospects. Under China’s current national immunization schedule, the final pre-school dose of meningococcal vaccination is administered at six years of age. For a long time, multivalent conjugate vaccine options for children over age three have been relatively limited in the domestic market. The newly approved expansion of the eligible age range helps address this gap, providing broader and more appropriate vaccination options for this population.At the same time, the broader eligible population is expected to further unlock Menhycia (R)’s commercialization prospects, and lay a more solid foundation for the product’s promotion and strategic rollout in international markets.Notably, CanSinoBIO issued its Results Forecast For The Year 2025 recently. Forecasting total revenue of RMB 1.04–1.08 billion, a year-on-year increase of 22.88% to 27.61% and net profit attributable to the shareholders of RMB 24.5–29.0 million—marking a return to profitability. The company noted that Menhycia (R), China’s first domestically developed quadrivalent meningococcal conjugate vaccine, continues to drive sustained revenue growth under its innovation-led commercialization strategy. This also signifies that the company is now reaping the commercial benefits of its early investments in vaccine innovation.Leveraging its proprietary platform, first-mover advantages, and accelerating global expansion, the age expansion of Menhycia (R) is expected to further strengthen CanSinoBIO’s competitive position while providing new momentum for sustainable growth. As product coverage broadens and international commercialization advances, the company is well-positioned to enter a new phase of long-term growth. Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月24日 - (亚太商讯 via SeaPRwire.com) - 2026年2月24日，康希诺生物（688185.SH/06185.HK）宣布，公司自主研发的ACYW135群脑膜炎球菌多糖结合疫苗（CRM197载体）——曼海欣(R)扩大适用人群的补充申请已正式获得国家药品监督管理局批准。此次获批后，曼海欣(R)适用于3月龄至6周岁（83月龄）的婴幼儿及儿童，用于预防由A、C、Y、W135群脑膜炎奈瑟菌引起的流行性脑脊髓膜炎（以下简称"流脑"）。此次曼海欣(R)扩龄获批，具有重要的公共卫生和商业发展意义。一方面，在我国现行免疫规划程序中，6岁是入学前流脑疫苗接种"最后一针"的重要节点，长期以来，国内针对3岁以上儿童的多价流脑结合疫苗选择相对有限。曼海欣(R)此次扩龄获批，为学龄期儿童提供了四价流脑多糖结合疫苗接种选择，有助于填补儿童流脑防控在关键年龄阶段的保护空白，进一步完善我国流脑免疫屏障。另一方面，适用人群范围的扩大，将有助于曼海欣(R)进一步释放产品潜力，提升商业化空间，并为该产品在国际市场的推广与布局奠定更为坚实的基础。值得一提的是，康希诺生物日前已发布2025年度业绩预告，全年营收预计10.4–10.8亿元，同比增长22.88%-27.61%；归母净利润预计2450万–2900万元，将实现扭亏为盈。同时，公告明确指出，"公司持续践行以创新为核心、以商业化落地为重点的发展战略，中国首款四价流脑结合疫苗曼海欣(R)收入保持持续增长"。这也意味着康希诺生物已进入创新疫苗商业化收获期。依托独家技术平台、领先优势及加速的国际化布局，曼海欣(R)扩龄不仅巩固了市场竞争力，也为康希诺生物的可持续增长注入新的动力。随着产品覆盖和国际拓展的推进，公司长期价值将开启更广阔的发展空间。 Copyright 2026 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月24日 - (亚太商讯 via SeaPRwire.com) - 2026年新版《道路机动车辆生产企业准入审查要求》中，仿真验证能力被作为强制性关键要素写入准入审查要求，国产仿真平台迎来巨大的市场利好，进一步推动了智驾产业链加速向"自主可控"迈进。在此背景下，五一视界宣布旗下51Sim下一代智驾仿真平台 SimOne 4.0 已于近日成功完成在摩尔线程旗舰级AI训推一体全功能GPU MTT S5000上的系统性适配与深度优化。从大模型感知挖掘、4DGS模型训练到4DGS仿真推理和合成数据生成，双方强强联手，实现了国产算力与端到端智能驾驶仿真体系的完整打通，正式开启了物理AI智驾领域高置信度闭环仿真与合成数据的全栈国产化新篇章,为应对新规下的严苛验证需求提供了坚实的国产底座。算力底座的"跨代式"追赶随着端到端智驾收敛到VLA和世界模型两条路线，基于海量Log数据的高置信度闭环仿真和合成数据已成为提升算法长尾场景处理能力的关键命题。仿真效率的上限，往往取决于基础一硬件的规格。在很长一段时间里，高端GPU市场几乎被海外巨头垄断，但五一视界与摩尔线程的最新合作成果显示，这一格局正在发生微妙的变化。SimOne 4.0已完成与摩尔线程MTT S5000的深度适配。MTT S5000是专为大模型训练、推理及高性能计算而设计的全功能GPU智算卡，基于第四代MUSA架构"平湖"打造。其单卡AI算力（稠密）最高可达1000 TFLOPS，配备80GB显存，显存带宽达到1.6TB/s，卡间互联带宽为784GB/s，完整支持从FP8到FP64的全精度计算。基于SimOne 4.0实现7个周视摄像头4DGS场景重建效果在实测数据中，MTT S5000展现出了足以抗衡甚至部分超越国际主流竞品的硬实力。数据显示，MTT S5000在FP32、FP16及INT8等关键精度上实现了约1.47倍的性能增长，FP64双精度算力领先幅度约1.48倍。更值得关注的是其搭载的MTLink技术，使得卡间带宽提升约30%。MTT S5000凭借FP8提升训推效率、FP64保障计算精准、光线追踪实现高保真渲染，以自主可控的强劲底层算力，为智能驾驶提供安全、高效、可靠的核心国产算力支撑。场景实测：在复杂博弈中验证"真功夫"硬件参数的领先，最终需要在真实的算法场景中落地。在SimOne 4.0的大模型感知挖掘功能中，双方针对Qwen3-VL多模态大模型进行了深度调优。实测结果令人惊喜：无论是在8B模型还是更复杂的30B MoE架构下，MTT S5000在"预填充（Prefill）"阶段的首字响应速度（TTFT）均优于国际主流竞品，优势最高扩大至14%，且在10并发的高压环境下依然保持了稳健的吞吐量。而在更考验训练和推理能力的4DGS（4D高斯泼溅）领域，基于51Sim入选AAAI 2026的LidarPainter技术，国产算力同样经受住了考验。目前测试数据显示，在训练端，MTT S5000展现出比肩国际主流竞品的强劲性能，仅需2.5小时即可完成一个真实Clip场景的高质量重建；在推理端，面对单Clip包含1600万个高斯点的超大模型负载，MTT S5000成功实现了11路摄像头加1路激光雷达的实时闭环仿真，呈现出像素级的高保真效果。这证明了国产显卡在处理复杂光影与动态物体还原时，已经具备了生产力级别的属性,能够胜任准入审查中要求的极端工况与边界条件验证。这种高保真物理场景的重建能力，同样可迁移至具身智能机器人的空间感知与操作训练中。基于LidarPainter 技术生成高真实度新视角图像隐形护城河：构建"芯片+系统"的通用底座如果说高性能GPU的适配是攻克了"最难的骨头"，那么对国产基础软硬件生态的全面覆盖，则是五一视界构筑的一条安全护城河,也是响应国家信创战略、满足敏感行业准入要求的关键。除了图形计算领域，五一视界已悄然完成了对主流国产芯片架构的全线互认。在CPU层面，无论是基于ARM架构的华为鲲鹏、飞腾，还是基于x86架构的海光、兆芯，五一视界旗下的51Aes、51Sim等核心产品均已实现流畅部署。特别是通过华为鲲鹏技术认证并加入"鲲鹏展翅"计划，进一步夯实了其在国产服务器端的运行稳定性。在操作系统层面，为了彻底摆脱对非国产发行版的依赖，五一视界将适配工作下沉至系统内核，先后完成了与麒麟软件（银河麒麟高级服务器操作系统）及统信软件（UOS）的适配认证。这一举措意味着，对于政府、能源等有着严苛信创要求的敏感行业客户而言，他们可以选择从芯片到底层操作系统到上层应用全链路自主可控的数字孪生解决方案,从容应对日益严格的合规性审查,构建起一个不仅服务于智能驾驶，更能广泛赋能于人形机器人等具身智能终端的国产化通用基础设施。中国科技企业"国产自主可控"已经崛起从携手摩尔线程在高端算力上撕开缺口，到打通华为鲲鹏、麒麟等操作系统的生态脉络，再到积极响应新版准入审查要求提供合规的仿真验证能力，五一视界的这一系列动作表明，中国企业的"国产自主可控"正在发生量变和质变，正在缓缓崛起。这不再是简单的参数对标，而是产业生态的战略闭环。SimOne 4.0的表现证明，国产软硬件方案已经迈过了"能用"的门槛，正式进入了高精度、高负载任务的"好用"阶段。随着算法与算力的深度融合，以及政策法规对仿真验证能力的强制加持，一个繁荣的、自主可控的物理AI生态底座正在逐步成型，为中国智能驾驶产业的独立发展保驾护航,也为具身智能机器人等新兴领域的国产化落地铺平了道路。基于SimOne 4.0 的4DGS闭环仿真 Copyright 2026 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

HONG KONG, Feb 24, 2026 - (ACN Newswire via SeaPRwire.com) – February 22, Galaxy Payroll Group Limited (NASDAQ: GLXG) (“Galaxy” or the “Company”), a Nasdaq-listed human resources solutions provider, today announced that it has formally renewed a five-year strategic cooperation agreement with NIKE China Holding HK Limited (Macau Branch) (“Nike Macau Branch”).Five-Year Renewal with Comprehensive HR Service CoveragePursuant to the agreement, the renewed cooperation term will commence on December 1, 2025 and continue through November 30, 2030. During this period, Galaxy will continue to provide Nike Macau Branch with a comprehensive suite of human resources outsourcing services, including local payroll processing, attendance and leave management, social security and tax compliance filings, as well as advisory services relating to labor regulations and employment policies.This integrated service model is designed to enable Nike Macau Branch to focus on its core retail and brand operations while enhancing overall organizational efficiency and compliance management.Strategic Renewal Reflects Client Confidence and Enhances Revenue VisibilityThe renewal marks an important milestone in the long-standing relationship between the parties and reflects the continued trust placed in Galaxy’s professional capabilities, compliance standards, and service delivery quality by a leading international brand.The execution of a multi-year agreement is expected to enhance the Company’s revenue visibility and cash flow stability over the next five years, further aligning with its capital markets strategy of building a high-quality, resilient, and sustainable business model. While the agreement provides for long-term cooperation, actual results may vary and remain subject to market and operational conditions.Local Expertise and Scalable Service Infrastructure as Core Competitive AdvantagesSince its establishment in 2013, Galaxy has focused on the Hong Kong and Macau markets while progressively expanding its cross-regional service capabilities. The Company has developed deep expertise in Hong Kong and Macau labor laws, taxation, and social security regulations, forming a strong local compliance foundation.Through a service framework that combines standardized operational processes with customized solutions, Galaxy delivers consistency and scalability across its client base. Its proprietary payroll and attendance management platform enhances operational efficiency while supporting data security and business continuity, serving as a key differentiator in attracting and retaining multinational enterprise clients.Throughout prior phases of cooperation, Galaxy has supported Nike Macau Branch in navigating complex employment and compliance environments. The Company’s solutions have demonstrated reliability in accuracy, responsiveness, and risk control, providing a solid foundation for this long-term renewal.Looking Ahead: From Service Delivery to Value Co-CreationEntering the new cooperation cycle, Galaxy intends to further optimize payroll workflows and intelligent attendance systems within the existing service framework. Through enhanced data integration and periodic management reporting, the Company aims to support the client’s ongoing efforts toward standardized and digitalized human resource management.The parties have also agreed to retain flexibility to expand the scope of services through supplemental agreements, enabling the partnership to evolve in alignment with the client’s business development.The renewal of this five-year strategic agreement not only represents long-term recognition of Galaxy’s professional value, but also underscores the sustainability of its business model. It is expected to further strengthen the Company’s brand presence in the Hong Kong, Macau, and broader Asia-Pacific human resources outsourcing markets, while serving as a replicable benchmark case for multinational retail, sports, and consumer brands.As global enterprises increasingly prioritize compliance efficiency, cost optimization, and organizational resilience, Galaxy continues to leverage its localized expertise, robust service infrastructure, and high-quality client base to build sustainable long-term growth momentum.The Company’s management commented: “We will continue to place service capability at the core of our growth strategy, deepen strategic cooperation with existing high-quality clients, and proactively expand relationships with multinational and regional enterprises that offer long-term value, with the goal of delivering steady and sustainable returns to our shareholders.”Contact informationJune TuoTel: (852) 5983-9260Phone: (86)1392-3804-279Intelligent Joy Limited Copyright 2026 ACN Newswire via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月24日 - (亚太商讯 via SeaPRwire.com) - 2026年2月22日, 纳斯达克上市公司迦里仕人才集团有限公司（Galaxy Payroll Group Limited，NASDAQ: GLXG，以下简称“迦里仕人才”）宣布，已与耐吉中国控股香港有限公司澳门分公司（NIKE China Holding HK Limited (Macau Branch)，以下简称“耐吉澳门分公司”）正式续签为期五年的战略合作协议。合作再延五年，服务范围全面覆盖核心HR职能根据协议，双方合作期限自2025年12月1日起至2030年11月30日止。在此期间，迦里仕人才将继续为耐吉澳门分公司提供涵盖本地薪资发放、考勤与休假管理、社保及税务合规申报，以及劳动法规与用工政策咨询在内的一站式人力资源外包服务。该合作模式有效支持耐吉澳门分公司聚焦其核心零售与品牌运营，提升整体组织效能。战略续约彰显客户高度信任，强化收入稳定性此次续约不仅是双方合作关系迈入新阶段的重要标志，更体现了国际头部品牌对迦里仕人才专业能力、合规水平及长期服务交付质量的高度认可。中长期合约的签署显著增强了公司未来五年收入的可预测性与现金流稳定性，进一步契合其打造高质量、抗周期业务模型的资本市场战略。本地化能力构筑核心壁垒，服务体系持续进化自2013年成立以来，迦里仕人才始终深耕港澳市场，并逐步拓展跨区域服务能力。公司凭借对香港及澳门劳动法、税务及社保政策的深度掌握，建立起扎实的本地合规能力；同时依托标准化流程与定制化方案相结合的服务体系，确保交付的一致性与可扩展性。其自主开发的薪资与考勤管理平台，在提升运营效率的同时有效保障数据安全与业务连续性，成为吸引并维系跨国企业客户的关键优势。在过往合作中，迦里仕人才已多次协助耐吉澳门分公司应对复杂用工环境下的合规挑战，其解决方案在准确性、响应速度及风险控制方面均获得充分验证，为本次长期续约奠定了坚实基础。展望未来：从服务交付迈向价值共创展望新合作周期，迦里仕人才将在现有服务框架基础上，持续优化薪资管理流程与智能考勤系统，并通过数据整合与定期管理报表，助力客户推进人力资源管理的规范化与数字化转型。双方亦约定保留通过补充协议灵活拓展服务范围的机制，确保合作节奏与客户业务发展动态同步。此次五年期战略合作的续签，不仅是对迦里仕人才专业价值的长期肯定，更是对其商业模式可持续性的有力印证。它将进一步巩固公司在港澳及亚太人力资源外包市场的品牌影响力，并为服务更多跨国零售、体育及消费品牌提供可复制的标杆案例。在全球企业日益重视合规效率、成本优化与组织韧性的背景下，迦里仕人才正凭借其深厚的本地化经验、稳健的服务体系与高粘性的优质客户基础，稳步构建长期增长动能。公司管理层表示：“我们将继续以服务能力为核心驱动力，深化与现有优质客户的战略合作，同时积极拓展更多具有长期价值的跨国及区域性企业客户，持续为股东创造稳健、可持续的回报。” Copyright 2026 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com

香港, 2026年2月24日 - (亚太商讯 via SeaPRwire.com) - 2月23日，由上海实业（集团）有限公司（以下简称"上实集团"）与国泰海通证券股份有限公司（以下简称"国泰海通"）联合发起设立的沪港新兴产业基石基金（以下简称"基石基金"）正式启航，进入实质投资阶段。作为全国首支、上海市级市场化运作的证券类港股基石基金，基金目标总规模30亿港元，首期规模10亿港元，将聚焦集成电路、生物医药、人工智能上海三大先导产业，专项支持优质企业赴港上市，深化沪港金融与产业协同。服务上海战略，强化沪港联动上海市政府和上海市国资委指导设立的基石基金，是上海国资服务上海科技创新中心建设、推动重点产业高质量发展的重要举措，将紧密围绕上海前瞻的集成电路、生物医药、人工智能三大先导产业进行战略布局，通过资本市场赋能，加速本地创新企业国际化进程。同时，基金也将充分发挥香港作为国际金融中心的枢纽功能，构建"上海产业+香港资本"的高效联通机制，促进两地金融资源互补与市场互联，打造沪港合作新标杆。创新"双管理人"架构，汇聚两地专业力量基石基金在治理模式上采用创新的"双管理人"架构，由上实集团在港金融投资业务平台上实资本（香港）投资管理有限公司，和国泰海通在港资产管理平台海通国际资产管理有限公司共同担任基金管理人，并由沪港两地协同运营。这一合作架构充分融合了上实集团作为上海在港窗口企业的产业资源与香港本地的运营优势，及国泰海通在全球资本市场和跨境资产管理方面的专业能力，实现"产业+金融"、"上海+香港"的双重优势互补。通过建立完善的投资决策机制与风险控制体系，该架构既确保了基金运作符合国际标准，又保持了与本土产业生态的深度链接，为基金的长期稳健运作奠定了坚实基础。多元化投资策略，专注长期价值基石基金坚持市场化、专业化、国际化运作原则，以产业、金融双重视角，构建覆盖企业全生命周期的投资与赋能体系。通过灵活的多元化策略组合与深度投后服务，系统性支持上海三大先导产业优质企业的业务发展与价值实现。基石基金在重点参与上海三大先导产业优质企业赴港IPO的基石投资之外，还可以参与港股IPO锚定和已上市港股的配售投资，通过无锁定期策略保持基金的流动性，以保证基金投资收益；在市场大幅下跌时，也可通过二级市场方式，增持价值低估的优质公司股票；同时跟进优秀企业再融资及并购重组，助力可持续发展。基石基金将严格遵循"好赛道、好公司、好价格"的遴选标准，重点投向具备核心技术、高成长性和稳健现金流的行业领军企业。强化上海国资在港功能，构建跨境投资新平台基石基金是上实集团和国泰海通强化在港服务功能、完善跨境投资布局的关键举措之一。基石基金不仅进一步完善上海国资基金矩阵，填补国资基金在港股IPO及二级市场策略的空白，服务上海企业赴港上市"最后一公里"融资需求，助力构建"早期投资—成长期融资—公开市场上市"的完整产业投资生态；更通过上实集团和国泰海通的深度合作，强强联手、协作共赢，系统提升跨境合规、资产配置与复杂交易设计能力，进一步增强上海国资服务上海乃至国家战略的综合实力。展望：链接国际资本，赋能创新未来在全球科技创新竞争日益激烈的背景下，沪港新兴产业基石基金的实质启动，标志着上海在对接国际资本市场、服务本土创新方面迈出系统性的一步。在人民币国际化和"惠港五条"等政策红利支持下，基石基金将成为连接内地产业资本与国际金融资源的重要纽带。未来，基石基金将积极把握人民币国际化与金融市场双向开放机遇，持续促进国际资本投资上海核心产业，为上海三大先导产业企业提供全方位的资本服务，助力更多硬科技企业走向世界，为沪港融合与高质量发展贡献力量。 Copyright 2026 亚太商讯 via SeaPRwire.com. All rights reserved. www.acnnewswire.com