▲提供需求定制或专项服务调研，请来电与专员沟通！！！ 【对接人员】：张 炜 精选部分目录 第一章 奥美沙坦酯制剂介绍 5 第一节 奥美沙坦酯制剂产品介绍 5 第二节 奥美沙坦酯制剂产品技术发展分析 6 第二章 中国与全球奥美沙坦酯制剂市场分析 9 第一节 中国与全球奥美沙坦酯制剂市场现状分析 9 一、中国奥美沙坦酯制剂市场现状分析 9 二、全球奥美沙坦酯制剂市场现状分析 10 第二节 2025-2031年中国与全球奥美沙坦酯制剂市场规模分析 12 一、中国奥美沙坦酯制剂市场规模分析 12 二、全球奥美沙坦酯制剂市场规模分析 13 第三节 2025-2031年中国与全球奥美沙坦酯制剂总产值分析 15 一、中国奥美沙坦酯制剂市场总产值分析 15 二、全球奥美沙坦酯制剂市场总产值分析 16 第四节 中国与全球奥美沙坦酯制剂行业发展前景分析 17 第三章 XXX公司简介 20 第一节 公司简介 20 第二节 公司产品介绍 21 第三节 公司发展优势分析 21 一、公司发展优势 21 二、公司研发优势 22 三、公司技术优势 22 四、公司专利优势 22 五、公司产品优势 24 六、公司品牌优势 25 第四章 奥美沙坦 ...

Group 1 - The company has made strategic acquisitions of Chang Le Pharmaceutical and Long Yi Pharmaceutical to enhance overall competitiveness through synergy, optimization of layout, complementary production lines, and cost advantages [1] - The acquisition of Long Yi Pharmaceutical aims to expand the CSO business and improve the pharmaceutical distribution sector, leveraging its market foundation and sales network in the Sichuan-Chongqing region to quickly increase local market share [1] - Post-acquisition, the company is focusing on improving efficiency through coordinated R&D project management and resource allocation, optimizing product layout to reduce costs, and integrating sales networks for resource sharing [1] Group 2 - The company is concentrating on innovative drugs, high-end formulations, and large-volume generic drugs, with a R&D team led by over ten PhDs and a planned R&D investment of approximately 277 million yuan in 2024 [1] - The company is innovating in sales by building a compliance system internally and enhancing market expansion externally [1] - The company is enhancing quality stability through intelligent transformation in production, with its new facility set to pass FDA inspections again in August 2024 [1] Group 3 - The company's core new drug LH-1801 (SGLT2 inhibitor) is in Phase III clinical trials, with 615 patients enrolled by January 2025, and the follow-up is expected to conclude in January 2026 [2] - LH-1801 shows significant synergistic effects for diabetic patients with hypertension, potentially opening a market worth 2 billion yuan upon approval in 2026 [2] - The prevalence of hypertension among adults in China is 31.6%, with the market for antihypertensive drugs dominated by sartans, which had sales of 2.2 billion yuan and 2 billion yuan for Irbesartan and Valsartan respectively in 2023 [2] Group 4 - The company recognizes the strategic value of centralized procurement policies for the pharmaceutical industry and has established a dynamic policy research mechanism to enhance its ability to respond to market changes [3] - The company aims to transform policy challenges into new opportunities for corporate transformation and upgrading through product structure optimization, accelerated innovation, and deepened cooperation with hospitals [3]

证券代码：002923 证券简称：润都股份 珠海润都制药股份有限公司 答：公司始终秉持"规范、专业、发展"的理念，以专注铸就卓越，以技 术引领未来。积极推动绿色化和合成生物技术的应用，加速仿制药与创新 药的研发与上市。公司将顺应医药行业发展趋势，重点围绕心脑血管、消 化系统、解热镇痛、手术麻醉用药等领域，做优做强制剂产业，持续保持 独具特色的药物新剂型和肠溶、 缓控释制剂技术优势，加快高技术壁垒 仿制药和原创新药研发上市，拓展全渠道终端，打造立体品牌。 6、原料药沙坦类价格趋势？ 答：随着公司全球化销售网络的稳步推进，大客户项目持续转化落地，沙 坦类产品销量不断攀升，进一步夯实了公司沙坦类产品的市场竞争力；受 供需关系等多重因素影响，沙坦类产品市场竞争依然激烈，市场销售价格 仍在低位区间波动。 | 关于本次活动 是否涉及应披 | | | --- | --- | | | 无 | | 露重大信息的 | | | 说明 | | | 附件清单 | 无 | | （如有） | | | | □特定对象调研 □分析师会议 | | --- | --- | | 投资者关系活 | □媒体采访 □业绩说明会 | | 动类别 | □新闻 ...

目 录 | 一、关于标的公司业务………………………………………………第 | 1—41 页 | | --- | --- | | 二、关于营业收入………………………………………………… 第 | 41—71 页 | 发行股份及支付现金购买资产暨关联交易 申请的审核问询函 之问询问题中有关财务事项的说明（修订稿） 天健函〔2025〕2-103 号 上海证券交易所： 由国投证券股份有限公司转来的《关于株洲千金药业股份有限公司发行股份 及支付现金购买资产暨关联交易申请的审核问询函》 （上证上审（并购重组） 〔2025〕23 号，以下简称审核问询函）奉悉。我们已对审核问询函所提及的株 洲千金药业股份有限公司（以下简称千金药业公司或公司）关于问询问题中有关 财务事项进行了审慎核查，现汇报如下。（除另有标注外，本说明的金额单位均 为万元，部分合计数与各单项数据之和在尾数上存在差异，这些差异是由于四舍 五入原因所致） 一、关于标的公司业务 根据重组报告书和评估报告：（1）千金湘江药业主要从事化学合成原料药 和固体制剂的研发、生产和销售，主要产品包括缬沙坦胶囊、盐酸地芬尼多片、 马来酸依拉普利片等 13 种产品；千金协力药业主要从 ...

Core Viewpoint - The ARB market is experiencing significant developments, particularly with the commercialization of the drug Benazepril by Lianhuan Pharmaceutical, which is expected to drive substantial revenue growth for the company [1][2]. Group 1: Market Position and Commercialization - Lianhuan Pharmaceutical has accelerated its market presence, with its Benazepril product already listed in 13 provinces as of June 30, indicating a rapid commercialization process [2]. - The drug is recognized as a first-line antihypertensive medication, with a strong clinical position and promising market prospects, potentially generating hundreds of millions in revenue for the company [2][3]. - The drug's core advantages include a breakthrough in receptor binding affinity, significant blood pressure reduction, and improved stability in blood pressure control, which enhance its market competitiveness [2]. Group 2: Research and Development Investments - Lianhuan Pharmaceutical has increased its R&D investment for three consecutive years, with a projected R&D expenditure of 277 million yuan in 2024, reflecting a year-on-year growth of 95.93% and surpassing 10% of its revenue for the first time [4]. - The company is advancing its core new drug LH-1801, which targets diabetes and hypertension, with clinical trials expected to conclude in early 2026, potentially opening a market worth 2 billion yuan [4]. Group 3: Product Portfolio and Strategic Positioning - Lianhuan Pharmaceutical has established a multi-layered product portfolio, including basic, combined, and innovative drugs, which strengthens its market position against competitors in the ARB market [6][7]. - The company is pursuing a "generic-innovative" strategy, which is crucial for its transformation into an innovative pharmaceutical enterprise, as it balances innovation with commercial viability [7].

7月2日晚美诺华（603538）披露业绩预增公告，公司预计上半年归母净利润同比增加142.84%到 174.52%，金额预计为4600万元到5200万元。扣除非经常性损益事项后，公司净利润同比增幅为55.80% 到86.33%。美诺华简要介绍，主要系本报告期内公司营业收入增加，毛利率提升所致。 美诺华是一家专业从事特色原料药和制剂研发、生产与销售的综合性国际医药科技制造型企业，核心产 品覆盖心血管、中枢神经、抗病毒、降血糖、胃肠消化道等治疗领域。作为国内出口欧洲特色原料药品 种最多的企业之一，美诺华与KRKA、默沙东、施维雅、吉瑞制药等国内外制药企业建立了长期深度稳 定的合作关系。 与一季度业绩对比，美诺华在二季度净利润增速有明显提升，一季度公司营收2.76亿元，同比增长 5.22%；净利润金额2122.17万元，同比增长51.12%。 不过从绝对金额来看，美诺华上半年4600万元到5200万元的利润区间，只是略高于2018年同期水平大 致，2018年之后的四年美诺华盈利表现逐年增长，直至2023年、2024年连续两年陷入回调。本次盈利增 长属于业绩的修复与释放。 据了解，此前公共卫生事件期间，由于全球原料短 ...

政策巨变下，姚俊华展现出技术出身的决断力。2019年，他力排众议启动"仿创双轮驱动"战略：每年拿 出销售额10%-16%投入研发，在南京、天津增设研发中心，组建260余人的研发团队（占员工总数 1/3）。当同行忙于分红时，他坚持将利润投入研发池。"仿制药是生存根基，创新药是未来命脉"，在 南通海门的车间里，这条理念正转化为现实：三条自动化生产线昼夜不停，最新获批的奥美沙坦酯氨氯 地平片单季度产量达500万片，17个仿制药新品去年密集上市，全国药企批文数量排名第十。 更重要的突破在实验室深处：首个创新药进入临床三期，预计2026年上市；20亿元的生物医药项目去年 3月落户海门开发区，为后续创新药量产铺路。"以前靠3-5个品种打天下的时代结束了，"姚俊华在一次 访谈中强调，"仿制药是马拉松补给站，创新药才是终点线。" 二、绿茵场上的健康方程式 夏夜的南通足球训练中心海门基地灯火通明，激情的浪潮在绿茵场上翻滚。当有球员带球突破时，场 边，一位目光严肃的中年人嘴角泛起欣慰的弧度——他正是万高药业掌门人姚俊华。此刻，实验室里的 药物研发专家、转型中的企业家、体育IP的塑造者三重身份在此交融，勾勒出一家药企的破圈生长轨 ...

润都股份（002923）公告，公司于2025年3月17日至2025年3月21日接受了巴西国家卫生监督局的现场 GMP认证，认证范围为化学原料药：坎地沙坦酯、沙库巴曲缬沙坦钠、替米沙坦、缬沙坦。近日，公 司收到巴西ANVISA签发的两张GMP认证证书，认证有效期至2027年5月26日和2027年6月9日。巴西 ANVISA现场检查结论为合格，即公司上述四个原料药产品均通过了巴西ANVISA现场GMP认证。 ...

港股晨报 港股回顾 点，跌幅随即扩大至 247 点，低见 23730 点，其后跌幅 一度收窄至仅 20 点，午后大盘走势偏软，尾盘沽压再 度扩大。截至收盘，恒指收报 23831 点，下跌 145 点或 0.61%；国指收报 9656 点，下跌 47 点或 0.49%，大市 成交进一步减至 827.99 亿。港股通录得净流入资金 4.84 亿，其中港股通(沪)净流入 2.83 亿，港股通(深)净 流入 2.01 亿。板块方面，本地地产、软件、5G 概念板 块跌幅靠前；黄金股逆市走强。 周四港股股指小幅调整，恒生指数收跌 0.61%报 24325.40 点，结束四日连涨，恒生科技指数跌 0.26%，恒生中国企业指数跌 0.63%。全日市场成 交额 2617 亿港元。南向资金净买入额 52.86 亿港 元。医药股领跌，荣昌生物跌近 12%。券商股冲 高回落，国泰君安国际跌超 4%。旅游股表现活 跃，香港中旅涨超 85%，成交超 75 亿港元。三只 新股表现分化，周六福、圣贝拉分别涨超 25%、 33%，颖通控股跌超 16%。 美股市场 1. 市场评估联储局官员减息预期，白宫称特朗普或 会延长关税暂停期限，美股周四高 ...

Core Viewpoint - The company successfully passed the FDA's cGMP inspection, which is a significant achievement that enhances its competitiveness and supports its expansion into the U.S. raw material drug market [1][2]. Group 1: FDA Inspection Details - The company underwent an FDA cGMP inspection from February 12 to February 17, 2025, focusing on the production of nine active pharmaceutical ingredients [1]. - The inspection covered various systems including quality, production, equipment, laboratory control, and material management [1]. - The company received the Establishment Inspection Report (EIR) confirming the successful completion of the inspection [1]. Group 2: Implications for the Company - Passing the FDA inspection establishes a solid foundation for the company's further expansion into the U.S. raw material drug market [2]. - This achievement is expected to inject momentum into the company's ongoing international market expansion efforts [2]. - The successful inspection is anticipated to enhance the company's overall competitiveness and promote future development [2].