SOUND SOLUTION FOR MANUFACTURING
A Global CDMO for Biologics
Dedicated End-to-End Solution
Quality System with Excellent Audit Track-record
Experienced Regulatory Support
ABOUT CHIME BIOLOGICS
Chime Biologics is a leading CDMO that enables its partners’ success in biologics. By leveraging our innovative R&D and manufacturing capabilities, we empower the entire biologics processes – from cell line development to commercial manufacturing – enabling customers to deliver affordable and accessible biologics that benefit patients worldwide.
With over 400 skilled employees, Chime Biologics leverages its comprehensive capabilities and internationally-recognized expertise to provide one-stop integrated solutions to worldwide customers. Relying on cell line development and advanced technology development from its Shanghai Innovation Center and proven success in IND-enabling through BLA filing at its Wuhan campus, Chime Biologics is providing high-quality pre-clinical, clinical and commercial manufacturing solutions.
Chime Biologics success is driven by reliable, compliant, flexible and fast-paced services from its innovative talent and operational excellence. We share a common goal to make cutting-edge biologics affordable and accessible to all patients globally, fulfilling its commitment to human health.
With over 400 skilled employees, Chime Biologics leverages its comprehensive capabilities and internationally-recognized expertise to provide one-stop integrated solutions to worldwide customers. Relying on cell line development and advanced technology development from its Shanghai Innovation Center and proven success in IND-enabling through BLA filing at its Wuhan campus, Chime Biologics is providing high-quality pre-clinical, clinical and commercial manufacturing solutions.
Chime Biologics success is driven by reliable, compliant, flexible and fast-paced services from its innovative talent and operational excellence. We share a common goal to make cutting-edge biologics affordable and accessible to all patients globally, fulfilling its commitment to human health.
KUBio, world's first modular biopharmaceutical factory
30+
Countries worldwide where
our products are supplied for clinical trial stage
~30
The executive team has an average of about 30 years of experience in the global biotechnology industry
50+
Successfully completed the production of over 50 batches of 2000L clinical samples (80+batches of GMP), mainly for Phase II/III trials
Our strategy focuses on providing end-to-end developing and manufacturing service empowering biotech companies around the globe to bring life-changing medicines to the market with expedite timeline. We will do this by:
- Focusing on Clients’ value — collaborating closely with our clients with greater agility and flexibility, achieving clients’ target goal and value success with mutual benefits.
- Achieving Operational Excellence — relentlessly striving to improve in all disciplines leveraging new technology and innovation, while ensuring global GMP compliance with our depth and breadth of experience and reliability of quality.
- Upholding highest degree of Integrity — strictly abiding by business integrity and professional compliance. Taking the uttermost care in protecting Clients’ Intellectual Properties right.
- Empowering our Employees — fostering the best platform to continuously encourage, empower and challenge all employees to be their best self.
Our fully-integrated one-stop platform provides the following functional services:
- Cell Line Development
- Process Development
- Process Transfer
- Quality Control and Assurance (QC/QA)
- Protein Science Characterization
- Clinical Manufacturing (DS/DP)
- Commercial Manufacturing (DS/DP)
- Material Management & Logistics
- Regulatory Support
Diverse Biologics Manufacturing Capabilities
- Monoclonal Antibody
- Bispecific Antibody
- Fusion Protein
- Conjugated Protein
- Enzymes
- Vaccine
CDMO SERVICES
We offer full suite of end to end CDMO services with exceptional efficiency and flexibility to meet your business needs. Our thorough knowledge of global regulatory compliance ensures the quality assurance of the drug substances and drug product manufactured. As of today, Chime Biologics has supplied clinical materials for various stages of clinical trials worldwide.
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