about us

CHENGDU SHENGNUO BIOPHARMACEUTICAL

Chengdu Shengnuo Biopharm Co., Ltd. (hereinafter referred to as “Shengnuo Biopharm”) is a wholly-owned subsidiary of Chengdu Shengnuo Biotechnology Co., Ltd. It was established in October, 2004 and is regarded as a "High-tech Enterprise Certified by Sichuan Province" and a "Sichuan Provincial Enterprise Technology Center". With a registered capital of 50 million yuan, it possesses over 50 key technologies for the large-scale production of peptides that have been marketed both domestically and internationally. It is a mature professional enterprise in China for the large-scale production of peptides and amino acid drugs, with a single batch output reaching the kilogram level and has passed the US FDA certification.

Chengdu Shengnuo Biopharm Co., Ltd. is a specialized, sophisticated, and innovative enterprise and a national high-tech enterprise specializing in the peptide field, which went public in 2021. We integrate R&D, production, and sales, with business covering peptide active pharmaceutical ingredients (APIs), cosmetic bioactive peptides, CDMO services, and peptide formulations. As a leading company in China's peptide API sector, we focus on the development, production, and technical services of peptide drugs, possessing full industrial chain capabilities from drug discovery to commercial manufacturing.

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2004

Company incorporation

5000 +

Capital of 50 million yuan

50 +

More than 50 key technologies

2000 +

Global partners

Peptide R&D Center

The center has been deeply involved in the field of peptides for more than 20 years, and has peptide API process research laboratories with a total area of 3,000 square meters, peptide API pilot plants with a total area of 1,500 square meters, GMP grade workshops for peptide API and topical drug development with a total area of 3,000 square meters, and drug development and analysis laboratories with a total area of 5,200 square meters. It has a professional R&D team of over 400 staff, and has successively carried out more than ten national and provincial scientific research projects, such as the National Major Special Project for Innovative Drug, covering multiple treatment areas including digestive system, immunity, tumor, hepatitis B, diabetes and obstetrics, and has obtained approval of more than 20 drugs, and plays an important role in promoting the development of China's peptide drug research and industrialization.

Four major production bases

Expert team

Expert Group for the Practice of Peptide Pharmacy Research

Innovative Drug and Generic Drug Development

Synthesis and Modification of Highly Complex Peptides

Purification of Complex Peptides

Synthetic Process Research and Optimization

Mass Production and Quality Control

Drug Application and Registration

An average of 15+ years of research and practical experience in peptide synthesis

Sichuan Province's top talent introduction of leading innovative and entrepreneurial teams

Provide CDMO services for more than 50 innovative drugs, several of which have been approved and marketed, and more than 30 of which are in clinical trials.

Lead 5 "Eleventh Five-Year" National Major Special Project for Innovative Drug: Atosiban Acetate, Octreotide Acetate, Somatostatin, Thymalfasin (thymosin alpha 1) and Carbetocin. All of them achieved commercially produce.

Completion of two domestic First Approved Generic Drugs: Enfuvirtide for injection and Carbetocin injection.

Complete the synthesis and mass production of several highly complex peptide drugs such as Liraglutide, Semaglutide, Tirzepatide and Enfuvirtide.

CORPORATE CULTURE

mission

Devoting to the peptide industry, safeguarding life and health.

vision

Innovation leads development, becoming the leader in the peptide industry.

core values

Customer first, win-win cooperation. People-oriented, co-creation and sharing.

Development History

2023

全球门户将于2024年进行全面升级和改造,以提升其应用性能和用户体验。此次升级旨在引入先进的技术和功能,以确保门户在全球范围内提供更为先进、高效和便捷的服务。通过这次改革,我们旨在满足用户不断增长的需求,为他们提供更加创新、智能化的在线体验。

2023

全球门户将于2024年进行全面升级和改造,以提升其应用性能和用户体验。此次升级旨在引入先进的技术和功能,以确保门户在全球范围内提供更为先进、高效和便捷的服务。通过这次改革,我们旨在满足用户不断增长的需求,为他们提供更加创新、智能化的在线体验。

2023

全球门户将于2024年进行全面升级和改造,以提升其应用性能和用户体验。此次升级旨在引入先进的技术和功能,以确保门户在全球范围内提供更为先进、高效和便捷的服务。通过这次改革,我们旨在满足用户不断增长的需求,为他们提供更加创新、智能化的在线体验。

2023

全球门户将于2024年进行全面升级和改造,以提升其应用性能和用户体验。此次升级旨在引入先进的技术和功能,以确保门户在全球范围内提供更为先进、高效和便捷的服务。通过这次改革,我们旨在满足用户不断增长的需求,为他们提供更加创新、智能化的在线体验。

2023

全球门户将于2024年进行全面升级和改造,以提升其应用性能和用户体验。此次升级旨在引入先进的技术和功能,以确保门户在全球范围内提供更为先进、高效和便捷的服务。通过这次改革,我们旨在满足用户不断增长的需求,为他们提供更加创新、智能化的在线体验。

2023

全球门户将于2024年进行全面升级和改造,以提升其应用性能和用户体验。此次升级旨在引入先进的技术和功能,以确保门户在全球范围内提供更为先进、高效和便捷的服务。通过这次改革,我们旨在满足用户不断增长的需求,为他们提供更加创新、智能化的在线体验。

2023

全球门户将于2024年进行全面升级和改造,以提升其应用性能和用户体验。此次升级旨在引入先进的技术和功能,以确保门户在全球范围内提供更为先进、高效和便捷的服务。通过这次改革,我们旨在满足用户不断增长的需求,为他们提供更加创新、智能化的在线体验。

International first-class production environment and equipment

Patents and Technologies

Global leading QA system

industry influence

Business coverage of partners and markets