Valteric Pharmaceuticals is a contract development and manufacturing organization (CDMO) delivering end-to-end pharmaceutical solutions. From early-stage formulation through commercial-scale production, we combine technical precision with rigorous regulatory compliance to bring therapies to market faster and more reliably.
Comprehensive pharmaceutical manufacturing capabilities under one roof
Pre-formulation studies, prototype development, and scalable formulation design for oral, topical, and injectable dosage forms.
Aseptic fill-finish operations with isolator technology for vials, pre-filled syringes, and lyophilized products.
High-speed tablet compression, encapsulation, and coating with capacity for clinical through commercial batches.
Primary and secondary packaging with full serialization and aggregation for global track-and-trace compliance.
Method development, validation, stability testing, and release testing with FDA-compliant laboratories.
Integrated sourcing, inventory management, and cold-chain logistics to ensure uninterrupted supply to global markets.
Regulatory excellence is the foundation of everything we do
US Food & Drug Administration
Current Good Manufacturing Practice
Quality Management Systems
Medical Device Quality
Quality is embedded in our culture, not just our processes. Every team member is trained to uphold the highest standards of pharmaceutical manufacturing, from raw material qualification through final product release. Our quality systems are designed for continuous improvement, ensuring we stay ahead of evolving regulatory requirements.
Experienced professionals driving pharmaceutical excellence
Operations Manager
VP of Quality
Dir. of Manufacturing
Head of R&D
Ready to discuss your pharmaceutical manufacturing needs?
San Diego, California
United States
Email: info@valteric.com
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