Join KBI Biopharma at the Colorado Protein Stability Conference to discover how our integrated Chemistry, Manufacturing, and Controls (CMC) expertise helps solve complex stability and developability challenges. From biophysical characterization and particle analysis to formulation development, process development, and manufacturing, KBI combines specialized scientific expertise with a comprehensive development strategy to help reduce risk and accelerate your path to the clinic.
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Meet with the KBI Biopharma Team:
Integrated Solutions: From biophysical characterization and particle analysis to formulation, process development, and manufacturing, KBI provides seamless CMC solutions that reduce risk, streamline development, and accelerate your path to the clinic. One partner. Integrated expertise.
Scientific Excellence: Discover advanced biophysical characterization, particle analysis, formulation development, and in silico formulation design that help optimize molecule stability, improve developability, and build confidence for regulatory success.
Flexible Service Options: Through KBI's Standalone Services Portal, access specialized analytical, formulation, and development expertise when and how you need it. Whether you need targeted scientific support or a fully integrated CDMO partner, KBI provides the flexibility to meet your program's unique needs.
Expert Consultation: Meet with KBI's scientists to discuss your protein stability and developability challenges, explore tailored solutions, and identify practical strategies to move your biologics program forward.
Ready to see how we accelerate biologics programs like yours? Stop by the booth or schedule a one-on-one meeting with our team.
About KBI Biopharma:
KBI Biopharma is a leading global contract development and manufacturing organization (CDMO) providing fully integrated, accelerated drug development and biologics manufacturing services and expertise to life science companies. With each of our 1400+ client partners, we work closely to personalize and accelerate drug development programs. Built upon a foundation of world-class analytics capabilities and extensive scientific and technical expertise, we deliver robust process development and clinical and commercial cGMP manufacturing services for mammalian and microbial programs. Recognized for quality manufacturing, we help clients advance drug candidates into the clinic and beyond.
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The Colorado Protein Stability Conference returns to Breckenridge, Colorado, from August 3–6, bringing together leading researchers from academia and industry to explore the latest advances in protein stability and biotherapeutic development. Since 1994, the conference has served as a premier forum for scientific exchange, with sessions covering protein aggregation, viral vector stability, therapeutic protein engineering, protein-excipient interactions, and emerging analytical approaches shaping the future of biologics.