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會議贊助商
1
2026 - 01 - 27
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北京映急醫藥冷鏈科技有限公司母公司成立于1999年，公司總部位于北京市通州區，注冊商標為“城市映急”，是一家干+倉+配管理一體化的專業醫藥冷鏈綜合解決方案服務商。為藥企、經銷企業、臨床研發企業、臨床服務及各類CRO提供一體化服務。城市映急專注醫藥冷鏈服務二十六年，在國家大力扶持生物醫藥行業等政策利好和監管加強的雙重驅動下，一直在探索求新，嚴格遵守醫藥冷鏈服務相關法律法規，堅持高標準的職業操守，率先自主研發物流與溫控監控系統，依托領先的溫控技術及通過國際認證的溫控設備，為眾多知名CRO和醫藥客戶提供信息化冷鏈管理服務，推動藥品上市，為人類大健康提供助力。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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吉瑪基因是由海歸學者團隊共同創辦的高科技生物技術公司，目前約有員工300人，場地面積13,000m²。公司長期專注于RNA領域，擁有一體化的RNA技術整合開發平臺，可以完成從RNA單體生產、oligo設計和合成、針對靶基因的高通量篩選、體內/體外評價等臨床前研究。核酸原料藥GMP生產車間和生產基地也能為未來的臨床研究、藥品注冊和商業化生產提供支持。公司的伴隨診斷包括熒光定量、質譜、RNAFISH三個技術平臺，同時建成了1,000m²的三類診斷試劑GMP生產車間。動物平臺有轉基因動物、CDX、PDX動物模型，還有配備有1,340m²的SPF級的動物房。吉瑪公司希望利用現有平臺為大型藥企盡快進入RNA藥物領域提供平臺和支持。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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太美智研醫藥研發(上海)有限公司(簡稱“太美智研醫藥”)，總部位于上海，是AI驅動的醫藥研發解決方案提供商。依托深厚臨床研究積淀，公司深度融合A 技術與創新模式，為全球藥械企業及科研機構提供國際品質的一站式臨床研究解決方案，以標準化運營與全流程賦能，構建高質合規、高效透明的研發體系，加速創新轉化。公司具備臨床早期至上市后全鏈條服務能力，業務覆蓋法規注冊事務、醫學事務、項目運營管理、統計分析與編程、數據管理、獨立評估、藥物警戒、患者招募及真實世界洞察。迄今已服務600余家藥械企業，開展1600余項臨床研究，覆蓋腫瘤、心血管、自免、內分泌、腎臟等多個治療領域。憑借全流程專業實力，助力多項關鍵臨床研究大幅縮短研發周期，推動新藥早日獲批上市。 公眾號二維碼: 公司網站: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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