上海精诚智研生物医药有限公司
About Us

Our Company

CIR Biopharma (Shanghai) Co., Ltd. has a senior R&D technical team, and its center management has more than 10 years of pharmaceutical and/or CRO working experience. The company jointly with the top research teams of Central South University, Ocean University of China, Fudan University, Hunan Cancer Hospital and others in China, around the technical requirements of market (customer) project, actively develops animal disease models with differentiated advantages to meet the different technical needs of customer projects. The company commits to improve the quality of R&D services, reduce the cycles and costs of drug R&D, and improve the research success rate.

10+years

R&D experience

500+

Disease models

70%+

Master or above degree
Leading Technology Platform

PROFESSIONAL TECHNOLOGY PLATFORM

backgrounds
ONCOLOGY, AUTOIMMUNITY, INFLAMMATION AND METABOLISM

Drug development technology service platform

The platform covers in vivo and in vitro pharmacodynamics, pharmacokinetics, Non-GLP toxicology studies, etc. The team has 200+CDX models, hundreds of PDX models and 50+ autoimmune and inflammatory models, and metabolic disease models. Among them, the pharmacodynamic services such as tumor pharmacological models (syngeneic model, CDX model, PDX model, orthotopic tumor model, tumor metastasis model), autoimmune and inflammatory animal model, humanized model, metabolic disease model and others, are the advantageous technologies.

The team has established a solid research quality system to ensure the authenticity, accuracy, integrity, traceability of test data, and the timeliness of delivery. The team's rich project experience will effectively help the partner's new drug R&D project.

The platform takes research and technological innovation as the guide to ensure the quality of R&D technology, commit to provide customers with high-quality and efficient R&D services, Help enterprises improve the drug research success rate, reduce the cycles and costs of drug R&D, and continuously improve research quality.

NEWS

LASTEST POST

喜报| 热烈祝贺上海精诚智研生物医药有限公司获得“科技型中小企业”认定

根据《科技型中小企业评价办法》(国科发政〔2017〕115号)和《科技型中小企业评价服务工作指引》(国科火字〔2022〕67号)的有关规定,上海精诚智研生物医药有限公司成功通过“科技型中小企业”认定。

09-06 2024

贺报| 热烈祝贺精诚智研合作伙伴赋生康FS-8002中美临床试验获批

热烈祝贺上海精诚智研生物医药有限公司合作伙伴赋生康(上海)生物科技有限公司自主研发的双功能融合蛋白FS-8002获得中美临床试验批准。2024年7月25日,中国国家药品监督管理局药品审评中心(CDE)官网公示,由赋生康自主研发的靶向肿瘤微环境的双功能融合蛋白FS-8002获得临床试验许可,拟开发适应症为晚期实体瘤。在此之前,今年3月27日,FS-8002已获得美国食品药品监督管理局(FDA)的临床试验批准。

08-21 2024

喜讯 | 热烈祝贺上海精诚智研生物医药有限公司顺利通过ISO 9001质量管理体系认证审核

上海精诚智研生物医药有限公司专业从事药物临床前研究技术服务,拥有资深的研发技术团队,核心管理层拥有10年以上药企和/或CRO工作经验。公司服务平台涵盖体内外药效学、药代动力学、Non-GLP毒理学研究等。为了进一步加快公司发展、不断提高对客户项目研发服务质量水平、满足客户项目更高的需求、提升客户的满意度,在公司全体人员共同努力下,于2024年08月16日顺利通过ISO9001质量管理认证机构专家全面、细致、严格的审核,获得GB/T19001-2016/ISO9001:2015标准质量管理体系认证证书,确认精诚智研研发团队技术服务水平、研究条件、研发管理符合ISO9001质量管理体系标准的要求,认证范围为药物临床前药效学、DMPK、Non-GLP毒理学研究等。

08-20 2024