美迪西波士顿第二座研发中心
研发中心实验室
作为在中国较早提供整套临床前批件申请同时符合中国GLP和美国GLP标准的CRO公司之一，美迪西自2016年在波士顿设立办事处以来，便逐步构建起国际合作网络，并于2023年底启用了首个研发中心。此次波士顿研发中心扩容，将显著提高美迪西的国际服务能力，这也是美迪西对全球新药研发领域深刻变化与客户需求快速增长的积极响应。
研
发
中
心
办
公
室
作为美迪西链接全球创新资源的核心枢纽，波士顿研发中心将承担起引领行业技术趋势的重任。在这里，美迪西将与全球顶尖的药企、知名大学及前沿研究机构携手合作，推动技术创新，助力创新药物研发。同时，该研发中心也将成为美迪西深耕美国市场、辐射全球的重要战略据点，助力公司在全球范围内拓展业务。
林庆聪 博士
美迪西执行副总裁兼美国公司总裁
“波士顿是世界级的生物医药创新中心，其丰富的人才优势与技术资源是美迪西在此深入布局的重要考量。在这里，美迪西将深度利用本土优势激发内部潜力，持续强化创新技术能力，并通过协同创新与跨界合作，共同探索药物研发的新领域、新路径，以更加高效、高质的药物研发服务回馈客户的信任与期待。”
陈春麟 博士
美迪西创始人&CEO
“波士顿第二座研发中心的投入运营，是美迪西拓展国际版图、深化市场渗透力的战略基石，也是向世界展示创新能力与服务品质的重要窗口。依托此研发中心，美迪西将更紧密地链接全球生物医药的创新生态，深入洞察行业的最新趋势与市场需求，持续推动技术革新与服务升级，致力于成为全球值得信赖的生物医药临床前综合研发服务CRO。”
右滑查看中文版
In August 2024, Medicilon USA Corp (Medicilon)officially commenced operations at its second R&D center in Massachusetts, USA. Research at the new facility will focus on animal models for PK/PD and toxicology studies. This milestone heralds Medicilon’s continued global business expansion.
Medicilon's U.S. R&D Center
The Lexington, MA location was chosen to enhance synergy and communication with industry partners
Medicilon aims to enhance its contribution to pharmaceutical innovation by harnessing the proximity to numerous top biotech companies and research institutions. The Lexington site provides critical research services, while ensuring smooth communication with both industry-based and academic drug development teams. Medicilon’s commitment to quality and innovation will keep its research partners competitive as new therapeutic technologies continue to emerge.
The U.S. R&D service matrix was upgraded to empower accelerated development of novel drug modalities.
The new laboratory supplements Medicilon’s diverse R&D platforms with cutting-edge resources. The research center utilizes advanced instrumentation and animal laboratories, leveraging a rich animal model library (including over 440 tumor efficacy models and over 250 non-tumor target research animal models). The site’s elite scientists perform efficacy evaluation of small molecule drugs and biologics, as well as pharmacokinetic evaluation and optimization. Studies are completed in compliance with ICH, NMPA, and FDA standards.
Since Medicilon began to provide preclinical filing applications that meet both Chinese GLP and U.S. GLP standards, the team has progressively built an international collaborative network. The initial presence in Boston was established in 2016, providing U.S. business operations. By 2023, Medicilon had already commenced local research projects for key partners in the U.S. The expansion of the Massachusetts R&D center will significantly enhance Medicilon's international service capabilities. This move mirrors Medicilon's proactive response to the continual changes in drug development trends.
Dr. Qingcong Lin
President of Medicilon USA
"Boston, with its top-tier pharmaceutical innovation and technological resources, is a strategic choice for Medicilon to enhance its presence. Medicilon will leverage local advantages to stimulate internal potential, strengthen technological capabilities, and explore new fields in drug development through innovation and collaboration."
Dr. Chunlin Chen
Founder and CEO of Medicilon
“Relying on the Boston R&D center, Medicilon will more closely connect with the global pharmaceutical innovation ecosystem and continuously drive technological innovation and service upgrades. We are committed to becoming a globally trusted comprehensive preclinical research service CRO in the pharmaceutical industry."
About Medicilon
Medicilon (stock code: 688202.SH) was founded in 2004 and is headquartered in Shanghai. Medicilon is dedicated to providing comprehensive preclinical drug research services to global pharmaceutical companies, research institutions, and scientific researchers. Medicilon's comprehensive one-stop services feature robust project management and cost-effective, efficient R&D services that accelerate clients' drug development processes. The services span the entire spectrum of preclinical drug research, including drug discovery, pharmaceutical research, and preclinical research. As of the end of June 2024, Medicilon has provided drug development services to over 2,000 global clients. Medicilon has been involved in the research and development of 490 IND-approved clinical and generic drug projects, fostering growth alongside high-quality clients both domestically and internationally. Medicilon will continue to leverage its global perspective, focusing on Chinese innovation, and contributing to human health!
免责声明：生物E药团队主要关注细胞与基因治疗领域最新进展、具有转化价值的生命科学基础研究以及生物医药行业资讯，本公众号所发布的文章仅作信息交流之用，文中观点不代表生物E药的立场，亦不代表生物E药支持或反对文中观点。本公众号发布的相关信息亦不构成任何价值判断、投资建议或医疗指导，如有需求请咨询专业人士投资或前往正规医院就诊。
版权声明
