On the journey of drug development, each collaboration is a profound test of professional competence and a severe test of professionalism. Recently, Medicilon USA Corp. (Medicilon) is honored to have received a thank-you letter from Jingye Medicine & Chemical Co., Ltd (Jingye Medicine) and was awarded the "Best Collaboration Award". This not only recognizes the professional capabilities and service level of Medicilon, but also reflects the result of the joint efforts and tacit collaboration between the two parties.
Jingye Medicine, as a secondary safety production standardization enterprise for hazardous chemicals, continues to demonstrate outstanding professional capabilities and profound industry accumulation in the fields of pharmaceutical raw materials, pharmaceutical intermediates and CDMO project services. In collaboration with Jingye Medicine, the Medicilon team has always upheld professionalism, closely collaborating with Jingye Medicine's process and analysis teams to jointly face and successfully overcome a series of technical challenges in the research and development process, ultimately ensuring the smooth progress of the project.
Currently, Medicilon has been involved in five projects with Jingye Medicine, with three of them are under development. These successful collaboration cases not only demonstrate the outstanding capabilities of both parties in the pharmaceutical research and development field, but also establish a solid foundation for future in-depth collaboration between the two parties.
In the field of APIs, Medicilon currently possesses cGMP-compliant production lines for APIs that meet the requirements for IND filing in both the United States and China. From preclinical small-scale synthesis and process development to commercial production, Medicilon integrates deeply with the entire supply chain system of enterprises, including research and development, procurement, and production. The production scales could be flexibly adjusted ranging from milligrams to kilograms. Meanwhile, Medicilon possesses a rigorous and experienced analysis and quality inspection team, providing precise analysis services and strict quality control throughout the project.
The Medicilon's Process Department not only provides clients with services in the R&D, analysis testing, and stability research of generic drugs, but also offers services for the R&D, production, analysis testing, and stability research of innovative drugs in Phase I and Phase II clinical trials, gradually transitioning from R&D process development to industrial commercial production, and from CRO to CDMO.
About Jingye Medicine
Jingye Medicine & Chemical Co., Ltd. was established in 1998 in the Suzhou High-tech Zone Incubator, mainly producing APIs, pharmaceutical intermediates, and CDMO project services. The company covers an area of nearly 80 acres, currently employing 282 people, and owns 9 commercial production workshops, including 3 GMP workshops and 1 CDMO workshop. The main products include intermediates for Pemetrexed, Quetiapine Hydrochloride, Quetiapine Fumarate, Paroxetine Hydrochloride, and Sitagliptin intermediates. In 2008, the company passed the ISO9001 Quality Management System Certification, ISO14001 Environmental Management System Certification, and ISO18001 Occupational Health and Safety Management System Certification. In 2014, it obtained the Jiangsu Province Safety Standardization Level II Certification. In 2021, it obtained the Drug Production License. So far, the company has 36 high-tech products, applied for 25 invention patents, and obtained 15 authorized patents. In 2023, Jingye Medicine achieved a production value of RMB 230 million.
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