李亚平对《苏州市科技创新促进条例》贯彻实施情况给予肯定，并结合前期调研和本次执法检查指 出《条例》实施中存在的问题。他强调，要深入学习贯彻习近平总书记对江苏、苏州工作重要讲话精 神，以更高站位坚决扛起创新促进职责使命，紧扣推动科技创新与产业创新深度融合重大要求，着力建 设具有全球影响力的产业科技创新中心和具有国际竞争力的先进制造业基地。要以更大力度聚力攻坚科 技创新关键环节，强化高能级平台建设，推进产学研深度融合，做实创新人才支撑，完善科技金融服 务，重视知识产权保护，加快推动更多创新成果转化为新质生产力。要以更广视野精心勾绘创新引领发 展蓝图，更好发挥苏州科创资源富集、应用场景丰富、市场腹地广阔的独特优势，在法治轨道上推进科 技产业创新深度融合。 市委常委、苏州工业园区党工委书记沈觅，市人大常委会副主任黄靖、陈嵘，党组成员蔡绍刚，秘 书长陈正峰参加执法检查。 昨天（9月12日），市人大常委会主任李亚平带队，对《苏州市科技创新促进条例》贯彻实施情况 开展执法检查。 宜联生物医药公司致力于开发具备国际竞争力的偶联药物。检查组认真听取企业新药发现、工艺开 发、临床开发等情况介绍。在国家第三代半导体技术创新中心，检 ...

Core Viewpoint - Kailaiying Pharmaceutical Group (Tianjin) Co., Ltd. has demonstrated strong growth and potential in the industry, as revealed during recent institutional research activities [1] Financial Overview - For the reporting period, the company achieved revenue of 3.188 billion yuan and a net profit attributable to shareholders of 617 million yuan, with a backlog of orders amounting to 1.088 billion USD [2] - Revenue increased by 18.2% year-on-year, while net profit grew by 23.7% [2] - Gross margin stood at 43.5%, up by 1.3 percentage points, and net profit margin was 19.4%, an increase of 0.9 percentage points [2] - Adjusted net profit margin reached 21.4%, reflecting a year-on-year increase of 5.4 percentage points [2] Business Segment Highlights - Small Molecule CDMO business generated revenue of 2.429 billion yuan, a 10.6% increase year-on-year, with a gross margin of 29.8%, up by 9.5 percentage points [3] - Emerging businesses, including peptides and small nucleic acids, saw revenue of 756 million yuan, representing a 51.2% year-on-year growth [3] - The company expanded its global market presence, adding over 150 new CDMO business clients during the reporting period [2] - Revenue from multinational pharmaceutical companies grew by 14.7%, while overseas revenue increased by 23.3% [2] - Revenue from small and medium-sized pharmaceutical companies rose by 21.6%, with domestic revenue up by 3.4% [2] Operational Developments - The small molecule business maintained steady growth despite industry challenges, with significant advancements in overseas capacity construction [3] - The company completed the delivery of 4 R&D projects and 1 production order for MNC clients, along with 285 QA audits [3] - The emerging business segment has a backlog of orders that increased by over 90% year-on-year, with over 40% from overseas [3] - The domestic market saw the approval of its first commercial peptide project in the weight loss sector [3] Future Outlook - For the first half of 2025, the company expects a revenue growth of 13% to 15% [4] - The company plans to enhance cost reduction and efficiency measures while increasing market expansion efforts, particularly in peptides, oligonucleotides, and conjugated drugs [4]

Core Viewpoint - Zhejiang Jiuzhou Pharmaceutical Co., Ltd. reported a revenue increase of 3.86% year-on-year for the first half of 2025, reaching approximately 2.87 billion yuan, with a net profit attributable to shareholders of approximately 525.83 million yuan, reflecting a 10.70% increase compared to the previous year [5][6][18]. Financial Performance - The company achieved total revenue of 2,870,947,333.22 yuan in the first half of 2025, compared to 2,764,279,820.31 yuan in the same period last year, marking a 3.86% increase [3]. - The total profit for the period was 650,314,797.16 yuan, up 17.20% from 554,870,663.04 yuan in the previous year [3]. - The net profit attributable to shareholders was 525,831,348.24 yuan, an increase of 10.70% from 474,988,640.43 yuan [3]. - The net cash flow from operating activities increased significantly by 164.50%, reaching 845,148,144.61 yuan [3]. Business Overview - The company operates as a leading Contract Development and Manufacturing Organization (CDMO), providing comprehensive pharmaceutical development and manufacturing services, including small molecule drugs, peptide drugs, conjugated drugs, and oligonucleotide drugs [4][5]. - The global CDMO market has shown robust growth, with a compound annual growth rate (CAGR) of 39.9% in China from 2018 to 2023, and is projected to reach 208.4 billion yuan by 2028 [4][5]. - The company has established long-term partnerships with well-known pharmaceutical companies, enhancing its reputation as a trusted partner in the global innovative drug development sector [4][5]. Technological Advancements - The company has developed multiple technology platforms, including continuous flow technology, chiral catalysis, fluorine chemistry, and biocatalysis, which are essential for enhancing its R&D capabilities [6][10]. - The company has successfully expanded its peptide and conjugated drug platforms, providing services for complex compound synthesis and meeting international regulatory standards for green production [12][13]. - The company has applied for numerous patents, reflecting its commitment to innovation and maintaining a competitive edge in the pharmaceutical industry [10][12]. Market Position and Strategy - The company has focused on expanding its customer base and deepening relationships with major clients, resulting in a steady increase in project orders and revenue from commercialized projects [5][15]. - The company has been recognized with multiple awards, including being listed among the top 20 CDMO companies in China for 2025, highlighting its industry leadership and commitment to quality [5][15]. - The company is actively participating in international conferences and exhibitions to enhance its brand visibility and expand its market reach [15].

Core Viewpoint - Bayer is committed to enhancing its focus and resource investment in China's innovation ecosystem, aiming to collaborate with local innovators to discover the next significant breakthroughs in drug development [1]. Group 1: Competition Announcement - Bayer China has officially launched the "Co-Creation New Drug" competition, inviting Chinese innovators and biotechnology companies to submit and showcase their innovative research pipelines, drug molecules, or new technologies with breakthrough potential [1]. Group 2: Target Therapeutic Areas - The competition focuses on several key therapeutic areas, including: - Precision Oncology - Precision Cardiorenal Diseases - Immunology & Inflammation [2]. Group 3: Research Pipeline Stages - The competition accepts submissions at various stages of the research pipeline, ranging from early pre-clinical candidate compounds (pre-PCC) to clinical proof of concept (clinical PoC) [2]. Group 4: Drug Molecule Forms - Eligible drug molecule forms include: - Biologics - Small molecules (SMOL) - Conjugated drugs (XDC) - Genetic medicine - Small nucleic acid drugs (siRNA) - Molecular glue - Other platform technologies [3]. Group 5: Evaluation Criteria - Submissions will be evaluated by a review committee composed of Bayer China's and global R&D and business development experts based on innovation level, key data, advancement speed, and alignment with Bayer's R&D strategy [4].