Science Driven.
Client Centric.

For more than 20 years, KBI Biopharma has been a leading biopharmaceutical Contract Development and Manufacturing Organization (CDMO).

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Experiencing Delays? Leave the Logistics to Us.

KBI Biopharma is a trusted CDMO partner, working hand-in-hand with hundreds of clients around the world. Partnering with KBI brings our years of integrated material solutions to your project. From resin to columns to our chromatography methods, we have built-in processes and material flows that meet the requirements of control regulations while protecting our clients from logistical delays.

8 Global Locations

Across the United States and European Union

15+ Annual INDs Supported

Across a diverse range of indications

3,000+ Projects Completed

With a proven track record of success

Hundreds of cGMP Batches

Manufactured at KBI

A Sense of Calm in Today's Regulatory Landscape

We’ve made a point to help our clients feel confidence in and supported by the CDMO they’ve selected. From start-ups to mature companies, KBI Biopharma can jump in at any stage and move directly into our menu of capabilities and technical feasibility, creating a roadmap for a painless logistical experience.

15 Years of Pressure-Tested Quality Systems and Regulatory Compliance
FDA/EMA Inspected Facilities
cGMP Ready Manufacturing Suites
Well Versed in First-in-Human Studies, Late-Stage Manufacturing, and Commercialization
Industry's Most Comprehensive Large Molecule Particle Characterization
High-Throughput Single-Use Technology
More than 200 Active Product Stability Studies

From gene through to cGMP manufacturing, we have the knowledge and experience to support projects of various scopes. Our robust project planning delivers accurate, dependable timelines to accelerate your results and translate innovation into impact.