BUCHANG PHARMA(603858)
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菏泽:深入实施创新驱动发展战略,推进科技创新与产业创新融合
Qi Lu Wan Bao· 2025-12-05 03:15
齐鲁晚报.齐鲁壹点周千清 12月4日,菏泽召开菏泽市"决胜'十四五'续写新篇章"系列主题新闻发布会(科技创新专场),菏泽市科技局党组书记徐静、市科技局发展规划科科长张一 凡、市科技局资源配置与科研诚信科科长周溦、市科技局高新技术发展及产业化科科长杨红岩,共同介绍为大家介绍"十四五"时期菏泽市科技创新发展成 效,并回答记者关心的问题。 "十四五"以来,在市委市政府正确领导下,在全社会共同努力下,菏泽市深入实施创新驱动发展战略,大力推进科技创新与产业创新深度融合,全市科技 创新取得突破性进展,为经济社会高质量发展提供了有力支撑。 科技管理体制实现重大变革,科技发展统筹作用显著增强 紧跟党中央和省委部署,加强党对科技工作的统一领导,成立中共菏泽市委科技委员会,统筹安排、协调部署全市科技创新重大战略任务、重点发展规 划、重要政策举措,实现了市县之间联动运转,部门之间协同配合,形成了全市科技工作"一盘棋"的发展格局。 科技基础条件实现夯实优化,科技创新能力加快提升 科技创新成果丰硕,新质生产力蓬勃发展 一是高新技术产业发展迅速。2024年底,高新技术产业产值占规模以上工业总产值的比重超42%,较2020年提高4.27个 ...
山东步长制药股份有限公司 关于全资子公司完成工商变更登记的公告
Zhong Guo Zheng Quan Bao - Zhong Zheng Wang· 2025-12-01 23:20
Group 1 - The company announced the completion of business registration changes for its wholly-owned subsidiary, Yangling Buchang Pharmaceutical Co., Ltd. [1] - The changes include an updated business scope, which now encompasses traditional Chinese medicine extraction, medical research and development, and solar power technology services [1] - The registered capital of Yangling Buchang is 158 million RMB, and the company was established on August 31, 2010 [1] Group 2 - The company reported that its wholly-owned subsidiary, Baoding Tianhao Pharmaceutical Co., Ltd., has received approval from the Hebei Provincial Drug Administration for changes to its drug production license [3] - The changes include the addition of new production lines and workshops, specifically for soft capsule production and oral solution production lines [4][5] - The production license is valid until July 7, 2030, and the company is authorized to produce various forms of medications, including ointments, tablets, and oral solutions [4][5]
防治流感,上市药企有什么“手段”?
Shang Hai Zheng Quan Bao· 2025-12-01 19:24
Core Insights - The flu positive rate in China has reached nearly 45%, indicating a significant rise in flu cases, with some provinces experiencing high epidemic levels [1] - Investors are closely monitoring the supply and sales of flu medications and vaccines from listed pharmaceutical companies, which are actively preparing to meet public health needs [1] Group 1: Drug and Vaccine Supply - Multiple listed companies have reported sufficient reserves of flu medications and vaccines, ensuring stable supply capabilities [2] - Renhe Pharmaceutical has initiated a priority supply mechanism for Oseltamivir, while Dajia Weikang has adjusted production capacity based on market demand [2] - The entire supply chain, including raw material suppliers like Rhine Bio, is collaborating to ensure a robust response to market needs [2] Group 2: Vaccine Development - Companies are focusing on flu vaccines as a key area for development, with several achieving significant progress by 2025 [3] - Zhejiang Tianyuan Biopharmaceutical's quadrivalent flu vaccine "Yufening" has been approved for sale, alongside its trivalent vaccine "Yuganning" [3] - Baike Bio has innovated with a freeze-dried nasal spray flu vaccine, which has been upgraded to a liquid form for easier administration [3] Group 3: Treatment Options - Companies are building a diverse matrix of flu medications to address various symptoms and treatment needs [5] - Zhongsheng Pharmaceutical is advancing the commercialization of Anladiwei tablets for treating uncomplicated influenza, while Jichuan Pharmaceutical is developing a novel flu treatment [5] - Oseltamivir remains a commonly used antiviral, with multiple companies like Renfu Pharmaceutical and Dajia Weikang actively involved in its production [5][6] Group 4: Symptomatic Relief - Several companies are providing symptomatic treatments for flu, including Lisheng Pharmaceutical's Acetaminophen and various products from Zhenbaodao for symptom relief [6] - Companies like Foci Pharmaceutical produce a range of cold and flu medications, ensuring comprehensive treatment options for patients [6]
步长制药:全资子公司完成工商变更登记
Zheng Quan Ri Bao· 2025-12-01 14:25
Core Viewpoint - Company announced a change in the business scope of its wholly-owned subsidiary, Yangling Buchang Pharmaceutical Co., Ltd., to meet operational management needs [2] Group 1 - The fifth meeting of the fifth board of directors is scheduled for November 7, 2025, to review the proposal for the change in business scope [2] - Yangling Buchang has completed the industrial and commercial change registration procedures and obtained a new business license from the Yangling Demonstration Zone Market Supervision Administration [2]
步长制药(603858) - 山东步长制药股份有限公司关于全资子公司完成工商变更登记的公告
2025-12-01 10:00
关于全资子公司完成工商变更登记的公告 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。 证券代码:603858 证券简称:步长制药 公告编号:2025-226 山东步长制药股份有限公司 经营范围:一般项目:中药提取物生产;医学研究和试验发展;非居住房 地产租赁;太阳能发电技术服务(除依法须经批准的项目外,凭营业执照依法自 主开展经营活动)。许可项目:药品生产;药品委托生产;药品进出口;药品批 发(依法须经批准的项目,经相关部门批准后方可开展经营活动,具体经营项目 1 山东步长制药股份有限公司(以下简称"公司")于 2025 年 11 月 7 日召开 第五届董事会第三十五次会议,审议通过了《关于全资子公司经营范围变更的议 案》,公司全资子公司杨凌步长制药有限公司(以下简称"杨凌步长")因经营管 理之需要,拟对经营范围进行变更。具体内容详见公司 2025 年 11 月 8 日披露于 上海证券交易所网站(www.sse.com.cn)的《关于全资子公司经营范围变更的公 告》(公告编号:2025-209)。 近日,杨凌步长已完成工商变更 ...
步长制药(603858) - 山东步长制药股份有限公司关于全资子公司药品生产许可证变更的公告
2025-12-01 10:00
证券代码:603858 证券简称:步长制药 公告编号:2025-227 山东步长制药股份有限公司 关于全资子公司药品生产许可证变更的公告 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")近日获悉全资子公司保定 天浩制药有限公司(以下简称"保定天浩")获得河北省药品监督管理局许可, 同意保定天浩《药品生产许可证》车间生产线、药品委托情况的变更,其他内容 不变,现将相关情况公告如下: 许可证编号:冀 20150057 一、药品生产许可证相关情况 企业名称:保定天浩制药有限公司 注册地址:河北省定兴县兴华东路 128 号 分类码:AhzBh 法定代表人:王益民 企业负责人:殷文忠 质量负责人:卢颖 生产地址和生产范围:河北省定兴县兴华东路 128 号:搽剂,软膏剂,片剂, 溶液剂(外用),乳膏剂,凝胶剂,灌肠剂,油剂,硬胶囊剂,颗粒剂,喷雾剂 (仅限注册申报使用)*** 山东省菏泽市中华西路 1668 号(山东步长神州制药有限公司):集团内共 用中药提取、颗粒剂*** 1 山东步长制药股份 ...
步长制药:保定天浩制药有限公司药品生产许可证变更
2 1 Shi Ji Jing Ji Bao Dao· 2025-12-01 09:41
Core Viewpoint - Company Baichang Pharmaceutical's subsidiary, Baoding Tianhao Pharmaceutical Co., Ltd., has received a renewed drug production license from the Hebei Provincial Drug Administration, allowing for changes in production lines and facilities, which is expected to positively impact the company's future operations [1] Group 1: License and Production Changes - The renewed drug production license includes the addition of a new workshop and production line located at 16 Bichang Road, Qindu District, Xianyang City, Shaanxi Province [1] - The new workshop is designated for soft capsule production, and the production line is for oral solution dosage forms, specifically Vitamin D drops [1] - The company has commissioned Shaanxi Baichang Pharmaceutical Co., Ltd. to produce Vitamin D drops with specific dosages, which currently do not have approval numbers [1] Group 2: Operational Impact - The changes in the drug production license are expected to optimize the company's production structure and maintain stable production capacity to meet market demand [1] - The license changes are anticipated to have a positive impact on the company's future operations [1]
山东步长制药股份有限公司 关于为公司全资子公司提供担保的公告
Zhong Guo Zheng Quan Bao - Zhong Zheng Wang· 2025-11-28 00:42
Group 1 - Company provided a guarantee of 80 million RMB for its wholly-owned subsidiary, Shaanxi Buchang Pharmaceutical Co., Ltd., in a loan agreement with Huaxia Bank [2][7] - The board approved a total financing limit of up to 6.92 billion RMB for 2025, with specific guarantee limits for subsidiaries based on their debt ratios [3][12] - As of the announcement date, the total amount of guarantees provided by the company and its subsidiaries was 2.296 billion RMB, accounting for 22.48% of the company's audited net assets as of the end of 2024 [14] Group 2 - The company’s wholly-owned subsidiary, Shandong Danhong Pharmaceutical Co., Ltd., signed a contract with Beijing Excellent Future International Pharmaceutical Technology Development Co., Ltd. for clinical trials of a new drug [17] - The total cost for the clinical trial is 60.338 million RMB, covering 480 cases, with provisions for adjustments based on the final sample size [19] - This contract is expected to enhance the company's drug research and development capabilities, potentially saving time and costs in clinical trials [34] Group 3 - The company’s subsidiary, Shaanxi Buchang, received approval for changes to its drug production license, allowing for the addition of a new production line for tablets [42] - The changes are anticipated to optimize production structure and maintain stable production capacity to meet market demand [43]
全国首例“医保价”脑机接口手术完成;李西廷增持迈瑞医疗股份
2 1 Shi Ji Jing Ji Bao Dao· 2025-11-28 00:20
Policy Developments - The State Council, led by Li Qiang, held a meeting to advance the provincial coordination of basic medical insurance [2] Medical Device Approvals - Yuhanglong received two medical device registration certificates for diagnostic kits related to primary biliary cholangitis and idiopathic membranous nephropathy, enhancing its product line in liver and kidney disease diagnostics [4] - Hengrui Medicine announced the approval of clinical trial notifications for five drugs, including the humanized anti-PD-L1 monoclonal antibody Abedilizumab, with total R&D investments amounting to approximately 1.1 billion yuan [5] Capital Market Activities - Mindray Medical's chairman, Li Xiting, plans to increase his stake in the company by 200 million yuan, having already purchased shares worth approximately 30 million yuan [7] - Huayu Pharmaceutical intends to establish a private equity fund focused on the biomedical sector, with an initial commitment of 150 million yuan from the company [8][9] Industry Milestones - The first brain-computer interface surgery in China was successfully completed, utilizing a device from Wuhan Zhonghua Brain-Machine Fusion Technology Co., with the procedure priced according to government regulations [11] Clinical Trials and Collaborations - Buchang Pharmaceutical's subsidiary signed a contract for clinical trials of a new product, with a total cost of approximately 60 million yuan, aimed at enhancing the company's drug development capabilities [12] - Jincheng Pharmaceutical terminated negotiations with Giskit Pharma B.V. regarding exclusive commercialization rights, with no financial impact expected [14]
步长制药(603858.SH):子公司签订《参附益心颗粒注册临床试验委托合同》
Ge Long Hui A P P· 2025-11-27 11:06
Core Viewpoint - Company signed a contract for clinical trial services for a new product, indicating a strategic move to advance its product pipeline and enhance market competitiveness [1] Group 1: Contract Details - The contract is between the company's subsidiary, Shandong Danhong Pharmaceutical Co., Ltd., and Beijing Excellent Future International Pharmaceutical Technology Development Co., Ltd. for the clinical trial of "Shenfu Yixin Granules" [1] - The total cost for the clinical trial is 60,338,000.00 yuan (including tax), covering 480 cases with a 20% dropout rate [1] - If the final sample size exceeds 520 cases, additional costs will be calculated at 108,890.00 yuan per case, with a supplementary agreement to be signed [1] Group 2: Cost Breakdown - The total cost includes various expenses such as CRO service fees, hospital fees, data management and statistics, SMO fees, and recruitment costs [1]