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会议赞助商
1
2026 - 01 - 27
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北京映急医药冷链科技有限公司母公司成立于1999年,公司总部位于北京市通州区,注册商标为“城市映急”,是一家干+仓+配管理一体化的专业医药冷链综合解决方案服务商。为药企、经销企业、临床研发企业、临床服务及各类CRO提供一体化服务。城市映急专注医药冷链服务二十六年,在国家大力扶持生物医药行业等政策利好和监管加强的双重驱动下,一直在探索求新,严格遵守医药冷链服务相关法律法规,坚持高标准的职业操守,率先自主研发物流与温控监控系统,依托领先的温控技术及通过国际认证的温控设备,为众多知名CRO和医药客户提供信息化冷链管理服务,推动药品上市,为人类大健康提供助力。The parent company of Beijing City Biopharmaceutical Cold Chain Technology Co., Ltd was established in 1999, with its headquarters located in Tongzhou District, Beijing. The registered trademark is "City Express." It is a total solution provider for healthcare cold chain specializing in dry storage, warehousing, and distribution management. The company offers comprehensive services to pharmaceutical companies, distributors, clinical research enterprises, clinical service providers, and various Contract Research Organizations (CROs).With 26 years of expertise in pharmaceutical cold chain services, City Express has thrived under China's supportive policies for the biopharmaceutical industry and enhanced regulatory oversight. The company pioneers innovation while strictly adhering to pharmaceutical cold chain regulations and maintaining high professional standards. As a trailblazer, it independently developed logistics and temperature monitoring systems, leveraging cutting-edge thermal control technologies and internationally certified equipment. By providing digital cold chain management solutions to leading CROs and pharmaceutical clients, City Express accelerates drug approvals and advances global healthcare initiatives.
2
2026 - 01 - 26
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吉玛基因是由海归学者团队共同创办的高科技生物技术公司,目前约有员工300人,场地面积13,000m²。公司长期专注于RNA领域,拥有一体化的RNA技术整合开发平台,可以完成从RNA单体生产、oligo设计和合成、针对靶基因的高通量筛选、体内/体外评价等临床前研究。核酸原料药GMP生产车间和生产基地也能为未来的临床研究、药品注册和商业化生产提供支持。公司的伴随诊断包括荧光定量、质谱、RNAFISH三个技术平台,同时建成了1,000m²的三类诊断试剂GMP生产车间。动物平台有转基因动物、CDX、PDX动物模型,还有配备有1,340m²的SPF级的动物房。吉玛公司希望利用现有平台为大型药企尽快进入RNA药物领域提供平台和支持。Genepharma is a high-tech biotechnology company founded by overseas scholars. At present, it has about 300 employees and a site area of 13,000m².The company has long been dedicated to the RNA field, boasting an integrated RNA technology development platform capable of handling preclinical studies from single RNA production, oligonucleotide design and synthesis, high-throughput screening for target genes, to in vivo/in vitro evaluation. The GMP manufacturing facilities and production bases for nucleic acid APIs also support future clinical research, drug registration, and commercial production.The companys companion diagnostics include three technology platforms: fluorescence quantitative, mass spectrometry and RNA FISH. At the same time, a GMP production workshop of 1,000m² for class III diagnostic reagents has been built.The animal platform has transgenic animals, CDX and PDX animal models, as well as an SPF level 1,340m² animal house.Genepharma hopes to use the existing platform to provide a platform and support for large pharmaceutical companies to enter the RNA drug field as soon as possible.
3
2026 - 01 - 26
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太美智研医药研发(上海)有限公司(简称“太美智研医药”),总部位于上海,是AI驱动的医药研发解决方案提供商。依托深厚临床研究积淀,公司深度融合A 技术与创新模式,为全球药械企业及科研机构提供国际品质的一站式临床研究解决方案,以标准化运营与全流程赋能,构建高质合规、高效透明的研发体系,加速创新转化。公司具备临床早期至上市后全链条服务能力,业务覆盖法规注册事务、医学事务、项目运营管理、统计分析与编程、数据管理、独立评估、药物警戒、患者招募及真实世界洞察。迄今已服务600余家药械企业,开展1600余项临床研究,覆盖肿瘤、心血管、自免、内分泌、肾脏等多个治疗领域。凭借全流程专业实力,助力多项关键临床研究大幅缩短研发周期,推动新药早日获批上市。 公众号二维码: 公司网站:www.taimei.comTaimei CRO is an Al-driven provider of pharmaceutical R&Dsolutions. LeveragingAl as the core driver, we deeply integrateclinical research expertise,Al technol-ogy, and innovative models to offer the industry a moreefficient, transparent, and high-quality intelligent solution. Thiscomprehensive delivery includes:Clinical Operations, Data Science, Medical Science, RegulatoryAffairs, Pharmacovigilance, Patient Recruitment andManagement Platforms, IndependentAssessment & Real-World Insights.We have supported over 600 pharmaceutical and medicaldevice enterprises, delivered more than 1,600 clinical studies,and spanned major therapeutic areassuch as oncology, cardiology, autoimmune, endocrinology,and nephrology. Our end-to-end expertise has drasticallyshortened R&D timelines for critical trials,accelerating the approval and launch of new drugs.
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