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CHIME BIOPHARMACEUTICALS: A Global CDMO for Biologics
CHIME Biopharmaceuticals Chime Biopharma is a leading Contract Development and Manufacturing Organization CDMO specialized in biologic products, enabling the advancement of innovative therapies worldwide. By leveraging our cutting-edge research capabilities and manufacturing expertise, we empower clients across the entire biologic lifecycle – from cell line development through to commercial manufacturing – facilitating access to life-changing medicines for patients globally.
With a team of over 400 dedicated professionals, Chime Biopharma harnesses its comprehensive capabilities and global industry experience to offer one-stop integrated solutions to our international customers. Our Shangh Innovation Center drives breakthroughs in cell line development and advanced technology applications, while the Wuhan campus boasts proven success from IND-enabling to BLA filing processes. Together, these hubs provide high-quality preclinical, clinical, and commercial manufacturing services.
Chime Biopharma's mission is to foster an environment that delivers reliable, compliant, flexible, and swift services through our innovative talent pool and operational excellence. Our shared goal is to make cutting-edge biologic therapies accessible for all patients across the globe, fulfilling our commitment to enhancing health.
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30+ Countries Served
~30 Years of Executive Team Experience
50+
Over 50 batches of 2000L clinical samples produced 80+ GMP batches, primarily for Phase IIIII trials
Our strategic approach focuses on providing -to- development and manufacturing services, empowering biotechnology companies globally to bring life-changing medicines to market more swiftly. We accomplish this through:
Client Focus: Collaborating closely with clients, we offer greater agility and flexibility to achieve target goals with mutual benefits.
Operational Excellence: Pursuing continuous improvement in all disciplines using innovative technology while ensuring global GMP compliance.
Integrity Assurance: Strictly adhering to business ethics and professional compliance, safeguarding Intellectual Property rights.
Employee Empowerment: Creating a platform that encourages our employees to reach their full potential.
Our fully-integrated service offering includes:
Cell Line Development
Efficient mammalian cell line development for transforming research into drug substances
Process Development
Proven track record of scaling up processes for robust and cost-effective solutions
Protein Science
Full spectrum of structural and functional analytical services to support the lifecycle of drug substance and product development
Technology Transfer
Flexible and efficient approach to ensure seamless technical transfer, leveraging our scientific expertise
Drug Substance Manufacturing
Adoption of modular facilities with single-use bioprocessing technology. Our KUBio facility meets international cGMP standards
Drug Product Manufacturing
State-of-the-art filling capabilities for final drug product formulation and aseptic processing designed for global quality standards
Quality Assurance System
Certifications demonstrating commitment to quality, integrity, and competency
Regulatory Support
Comprehensive support for global regulatory applications ensuring reliable supply chn and consistent high-quality assurance
Project Management
Striving to provide superior project services fostering long-term relationships with our clients
Data Integrity
Integration of technology innovation in the quality management system to ensure data authenticity, completeness, and accuracy
Client Confidentiality Policy
Upholding strict business integrity and professional compliance standards. Protecting your rights is paramount.
CHIME Biopharma 2024 Excellence Awards - Award Detls
Going Global: Chime Biopharma's Journey to Innovation and Quality - Article Content
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