Group 1: Investor Relations Activity Overview - The investor relations activity was an earnings briefing held on May 27, 2025, at the China Securities Network "Roadshow Center" [4] - Participants included the company's chairman, general manager, and other key executives [4] Group 2: Key Financial Metrics - The company's R&D investment for 2024 is 12.01% of its revenue [5] Group 3: Market Management Strategies - The company plans to enhance its market value management through improved information disclosure and operational efficiency, while considering cash dividends, share buybacks, and mergers as part of its strategy [6] Group 4: International Certifications and Market Expansion - The company has received EMA certification for its "small-volume injection" workshop and FDA certification for "Docetaxel Injection," but currently has no other products submitted for international certification [7] - As of now, the company has not signed any overseas business orders, citing various uncertainties affecting international market expansion [7] Group 5: Product Portfolio and Sales - By the end of 2024, the company holds approximately 100 drug approvals, focusing on gastrointestinal, neurological, oncology, immunomodulatory, and cardiovascular treatments [9] - Top-selling products include compound digestive enzyme capsules, octreotide injections, and mecobalamin tablets [9] Group 6: Production Capacity and Project Updates - The "High-end Drug Formulation Processing Base Project" in Nanjing is under construction and has not yet commenced production [10] - Current production capacity at existing bases in Beijing and Guangdong meets business needs, with ongoing market expansion efforts [10] Group 7: Research and Development Progress - The company is currently in the review stage for its Oseltamivir oral disintegrating tablet, having submitted updated clinical data [11] Group 8: Financial Strategy - The company has no plans for mergers or acquisitions at this time, maintaining a low debt ratio [12]

Core Viewpoint - The company has made significant progress in product approvals and innovation, enhancing its market position and revenue potential in the pharmaceutical industry. Group 1: Product Approvals and Sales - In 2025, the company received multiple product approvals, including Mecobalamin tablets and enteric-coated Aspirin tablets, which will enrich its product line in the nervous system category [1] - The sales revenue for Mecobalamin tablets in Chinese public medical institutions was approximately 1.431 billion yuan in 2023, while the sales for enteric-coated Aspirin tablets reached about 3.3 billion yuan [1] Group 2: Research and Development - The company is focusing on R&D in various therapeutic areas, including cardiovascular, analgesics, digestive system, anti-metabolic, nervous system, and narcotic drugs, with over 100 drugs in the development pipeline [2][3] - It has established multiple large R&D platforms and is advancing several first-class innovative drugs, such as OAB-14 for Alzheimer's treatment [2] - The company emphasizes collaboration with academic institutions and has partnerships with over 50 domestic and international research organizations [3] Group 3: Financial Performance - In Q1 2025, the company reported a revenue of 2.43 billion yuan and a net profit of 112 million yuan [4] - For the year 2024, the total revenue was 8.466 billion yuan, reflecting a year-on-year growth of 4.51%, while the net profit was 470 million yuan, slightly declining due to price reductions aimed at market capture [4] - The company plans a high dividend distribution, proposing a payout of 2.5 yuan per 10 shares (including tax) for 2024 [4]

Core Viewpoint - Xinhua Pharmaceutical (000756) has received approval from the National Medical Products Administration for the supplementary application of Mecobalamin tablets, allowing the transfer of the marketing authorization holder [1] Company Summary - The transaction does not require approval from the company's board of directors or shareholders, as it does not constitute a related party transaction or a major asset restructuring as defined by relevant regulations [1] - Mecobalamin tablets are indicated for peripheral neuropathy and are listed as a Class B drug in the National Basic Medical Insurance, Work Injury Insurance, and Maternity Insurance Drug Catalog [1] Industry Summary - In 2023, the sales revenue of Mecobalamin tablets in Chinese public medical institutions is approximately RMB 1.431 billion [1]

山东步长制药股份有限公司 证券代码：603858 证券简称：步长制药 公告编号：2025-061 关于全资子公司经营范围变更的公告 本公司董事会及全体董事保证本公告内容不存在任何虚假记载、误导性陈述或者重大遗漏，并对其内容 的真实性、准确性和完整性承担法律责任。 山东步长制药股份有限公司（以下简称"公司"）于2025年4月2日发出第五届董事会第十九次会议的通 知，并于2025年4月9日13时以通讯方式召开，会议以同意9票、反对0票、弃权0票的表决结果审议通过 了《关于全资子公司经营范围变更的议案》，公司全资子公司保定天浩制药有限公司（以下简称"保定 天浩"）、陕西步长制药有限公司（以下简称"陕西步长"）因经营管理之需要，拟对经营范围进行变 更。具体情况如下： 一、变更情况 （一）保定天浩 截至2023年12月31日，资产总额48,863.12万元，负债总额31,996.87万元，净资产16,866.25万元，2023年 度实现营业收入121,474.02万元，净利润15,636.25万元。（上述数据经审计） 截至2024年9月30日，资产总额43,242.74万元，负债总额28,880.48万元，净资产14, ...

Core Viewpoint - The announcement indicates that Harbin Zhenbao Pharmaceutical Co., Ltd., a wholly-owned subsidiary of Zhenbao Island (603567), has received approval from the National Medical Products Administration for the transfer of marketing authorization for ten drugs from Anhui Jiuzhou Fangyuan Pharmaceutical Co., Ltd. to Harbin Zhenbao Pharmaceutical Co., Ltd. This change is not expected to have a significant impact on the company's current operating performance [1]. Group 1 - The approval includes the transfer of marketing authorization for ten drugs, which are Olanzapine Tablets, Apixaban Tablets, Escitalopram Oxalate Tablets, Desloratadine Tablets, Voriconazole Tablets, Mecobalamin Tablets, Rivaroxaban Tablets, Valsartan Tablets, and Donepezil Hydrochloride Tablets [1]. - The change in marketing authorization holders is a strategic move for Harbin Zhenbao Pharmaceutical Co., Ltd. to consolidate its product portfolio [1]. - The company emphasizes that this regulatory approval will not materially affect its current financial performance [1].

北京市北京经济技术开发区中和街 18 号 北京星昊医药股份有限公司 北京星昊医药股份有限公司招股说明书（注册稿） 本次股票发行后拟在北京证券交易所上市，该市场具有较高的投资风险。北京证券交易所主要 服务创新型中小企业，上市公司具有经营风险高、业绩不稳定、退市风险高等特点，投资者面临较 大的市场风险。投资者应充分了解北京证券交易所市场的投资风险及本公司所披露的风险因素，审 慎作出投资决定。 保荐机构（主承销商） 申万宏源证券承销保荐有限责任公司 新疆乌鲁木齐市高新区(新市区)北京南路 358 号大成国际大厦 20 楼 2004 室 证券简称： 星昊医药 证券代码： 430017 本公司的发行申请尚未经中国证监会注册。本招股说明书申报稿不具有据以发行股票的法律效 力，投资者应当以正式公告的招股说明书全文作为投资决定的依据。 中国证监会和北京证券交易所对本次发行所作的任何决定或意见，均不表明 其对注册申请文件及所披露信息的真实性、准确性、完整性作出保证，也不表明 其对发行人的盈利能力、投资价值或者对投资者的收益作出实质性判断或者保证。 任何与之相反的声明均属虚假不实陈述。 根据《证券法》的规定，股票依法发行后，发行 ...