Purity and Compliance for Pharmaceutical Innovation.
We manufacture ingredients designed to meet stringent USP and other global pharmacopeia standards, with batch-specific Certificates of Analysis available for every shipment.
Our processes ensure the precise molecular composition required for predictable therapeutic outcomes and bioavailability, batch after batch.
We provide ingredients and documentation that give our partners confidence for distribution across international healthcare markets, backed by rigorous in-process quality control.
Bio-Based Glycine USP
Renewable-origin, USP-grade Glycine for APIs, excipients, and critical formulations.
Glycine USP
High-purity, USP-grade Glycine for APIs and critical formulations.
Taurine
A stable, high-purity amino acid for pharmaceutical and nutraceutical applications.
Base
A high-purity intermediate for active ingredient synthesis.
A versatile intermediate for pharmaceutical synthesis.
Pharmaceutical-grade intermediate for API synthesis and antioxidant drug development.
Contact UsWe supply USP-grade Glycine (AviGly HP and Bio HP), Taurine (AviTau), Chlorhexidine Base, Guaiacol, and MEHQ for API synthesis, excipients, and specialty pharmaceutical intermediates, each backed by pharmacopeial-aligned documentation.
Pharmaceuticals customers should review alignment to USP and other global pharmacopeia standards, precise molecular composition for predictable bioavailability, batch stability data, and elemental impurity documentation before commercial approval.
Our certified manufacturing environment provides comprehensive documentation, including specification, CoA format, SDS, and stability data, supporting a smooth path to market for API, excipient, and nutraceutical registrations.
