查尔斯河实验室与驾玉生物合作,扩大生物制药服务的能力
威尔明顿,马萨诸塞州和上海,2021年1月14日消息—查尔斯河实验室(NYSE:CRL)宣布,已与生物制药行业端到端质量管理服务商——驾玉生物(JADE Biomedical)达成战略合作伙伴关系。该合作伙伴关系将扩大Charles River的生物制品检测能力,并有助于满足其对于生物制药产品(尤其是细胞和基因疗法)的需求,从而重申了公司作为全球发展合作伙伴的承诺。这一战略关系也将促使驾玉生物目前位于上海的国际cGMP标准生物大分子产品检测业务加速扩展到中国的第二个实验室,并进一步扩展驾玉完整的生物制药质量技术承包和检测业务。
随着全球生物制药行业的快速发展,对可靠的专业合同服务商的需求也在不断增长。细胞和基因治疗市场的商业化发展需要用科学和专业的质量管理知识来驾驭全球复杂的监管环境。驾玉生物凭借其对全球趋势和当地环境的深刻理解,以及其旨在为支持全球各种规模的客户(从本地初创企业到全球大公司)提供的商业运营模式,成为Charles River全球生物制品服务链中及其重要的一员;同时,将于今年夏天上线的第二个检测实验室,也将进一步提高驾玉生物基于客户不断增长的需求而提高其cGMP和GLP检测能力及规模。
关于双方的合作
Birgit Girshick, Charles River公司执行副总裁,负责生物制剂测试解决方案和禽流感疫苗服务的研发和安全评估工作。
— Claudia Lin博士,驾玉生物创始人兼首席执行官
关于Charles River
Charles River为全球的制药和生物技术公司提供必需的产品和服务,以加快其药物研究和开发工作。我们敬业的员工致力于以客户的切身需求为出发点而提供服务,从而促进和改善新疗法的发现、早期研发和安全生产工作,并最终服务于患者。欲了解我们独特的产品组合和广泛的服务,请访问www.criver.com。
联系方式
Charles River投资者联系人 Todd Spencer
公司投资者关系部副总裁 781-222-6455
todd.spencer@crl.com
Charles River媒体联系人 Amy Cianciaruso
公司公共关系副总裁 781-222-6168
amy.cianciaruso@crl.com
关于驾玉生物
驾玉生物为全球的生物制药公司提供专业的质量、法规和分析检测服务。作为世界上首家登记注册的生物制药合同质量组织Bio-CQOR,驾玉生物的服务模块包括质量保证,产品质量管理,药品注册申报,QC方法验证和检测、CMC和分析方法开发指导、厂房设施设计和验证、冷链管理等。驾玉生物的创始人和领导团队均为在大分子药物开发及生产质量管理方面与NMPA、FDA、 EMA、PMDA和PICS合作有着丰富经验的行业精英。我们依靠不断壮大的专业团队,通过为客户提供灵活而可靠的定制化质量和CMC系统并领导具体实施来支持客户从IND前到上市后的产业化过程。驾玉生物的合同检测服务可提供适用于全球先进cGMP标准兼容的实验室分析检测服务,支持国际化产品申报需求。我们的专业知识涵盖包括单克隆抗体,抗体欧联物,细胞和基因治疗等各种产品类型。欲深入了解驾玉生物及当前的招聘职位,请访问http://www.jade.bio/
联系方式
驾玉生物投资联系人 Claudia Lin 林巧 CEO
claudialin@jadebiomedical.com
驾玉生物媒体联系人 James Vang 市场拓展总监
jamesvang@jadebiomedical.com
Charles River Partners with JADE Biomedical
to Expand Biologics Capabilities
Strategic partnership demonstrates Charles River’s commitment as a global partner
WILMINGTON, MA and SHANGHAI, January 14, 2021 – Charles River Laboratories International, Inc. (NYSE: CRL) announced today that it has entered into astrategic partnership with JADE Biomedical, a provider of end-to-end quality management services for the biopharmaceutical industry. The partnership will expand Charles River’s biologics testing capabilities geographically and help to accommodate demand for biologics therapeutics, especially cell and gene therapies, reaffirming the company’s commitment as a global development partner. This strategic relationship will also enable JADE Biomedical to expand their current global cGMP product testing operations in Shanghai into a second facility in China and further build upon its current offering of comprehensive biologics quality management and testing services.
As the biologics therapeutics industry across the globe continues to grow at a rapid pace, so does the demand for a reliable, contract services partner. The recent growth in commercialization effort in the cell and gene therapy market requires both scientific and regulatory expertise to navigate the complex, global regulatory environment. JADE Biomedical’s deep understanding of the global trend and local environment, and its infrastructure designed to support clients of all sizes – from localstart-ups to global organizations, makes it a highly valuable addition to Charles River’s network. The addition of a second testing facility, which will come online later this year, will provide additional capacity to better support clients’ growing needs. The new facility will offer Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) services to clients.
Approved Quotes
Around the world, R&D efforts for cell and gene therapies are in high demand. Companies are seeking global partners who understand the complexities of this market, while also knowing how to navigate the nuanced regulatory environment in their region. Working with JADE Biomedical, we will be able to combine our expertise to provide localized knowledge with a deep scientific and regulatory network, positioning both organizations as go-to partners for clients in this competitive market.
– Birgit Girshick, Corporate Executive Vice President, Discovery and Safety Assessment, Biologics Testing Solutions, and Avian Vaccine Services, Charles River
JADE Biomedical was founded with the purpose of serving the growing needs of the biopharmaceutical industry, not only in China, but internationally. JADE Biomedical’s contracted Biologics Quality Organization, Bio-CQO®,
where end-to-end quality and regulatory technical services are provided is an important addition to the biologics outsourced services industry, filling gaps in shortage of expertise and leadership in quality and compliance. We are extremely grateful to the conducive regulatory environment in recent years in China, and the trust of leading, global biopharmaceutical companies that have allowed us to form a unique service model and brand. To continue our growth in biologics therapeutics, especially in the gene and cell therapy space, we needed a partner with global reach. With an industry-leading portfolio of services and regulatory expertise, Charles River will help us support an increasing number of clients globally and locally.
– Claudia Lin, PhD, Founder and CEO, Jade Biomedical
About Charles River
Investor Contact for Charles River:
Todd Spencer
Corporate Vice President, Investor Relations
781-222-6455
todd.spencer@crl.com
Media Contact for Charles River:
Amy Cianciaruso
Corporate Vice President, Public Relations
781-222-6168
amy.cianciaruso@crl.com
About Jade Biomedical (JADE)
Investor Contact for JADE Biomedical:
Claudia Lin
Founder & CEO
Media Contact for JADE Biomedical:
James Vang
Business Development Director
jamesvang@jadebiomedical.com