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Contract Biopharmaceutical Development
Contract biopharmaceutical development is the fastest-growing part of our business. Vybion scientists bring years of development and regulatory experience to every project and its challenges. Technology access through ProCode™ Technology can:
- Add significant value
- Cut long-term costs with higher yields
- Increase bioactivity
- Accelerate time to market
Quality Control
- GLP compliant
- Full analytical validation capabilities
- Detailed documentation of the development process
GMP
- Comprehensive planning from early development through phase I/II manufacturing
- Products developed at Vybion currently in all phases of clinical trials
Responsiveness
- Individual attention
- Project planning teams
- Adherence to milestones and timelines
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What Clients Can Expect
We work with our clients and partners to- Explore fully the properties of their proteins
- Develop specifications
- Define analytical requirements
- Provide accelerated stabilities studies
- Provide full service development through phase I/II manufacturing
- Furnish API, and final formulation release with validated methods
Protein Development Timeline
