Utide Pharmaceutical
Professional Peptide
API Manufacturer
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Our Core Capabilities
1500 Kilograms Annual Capacity
Utide operates a 14,000 m² production facility with integrated peptide synthesis, purification, and isolation capabilities. Leveraging advanced SPPS technologies, flexible reactor scales, automated synthesis, industrial prep-HPLC, precise salt exchange, and large-scale lyophilization, we deliver reliable scale-up and long-term peptide API supply with consistent batch quality.
Rigorous Quality Management
At Utide, quality is embedded throughout the entire peptide API lifecycle, from raw material qualification to final batch release. Our Quality Management System ensures robust governance, full traceability, and effective process control through comprehensive QA oversight and rigorous QC testing.
International Certification Schedule
Supported by an established DMF track record, our quality system is structured to align with global regulatory expectations, with GMP compliance advancing under a defined certification roadmap.
R&D-Driven Custom Peptide Solutions
Building on strong R&D foundations and deep expertise in peptide chemistry, our custom peptide solutions are designed to cover sequence design, diverse modification strategies, precise salt form and counter-ion control, application-matched purity, and comprehensive impurity profiling, ensuring consistent quality, reproducibility and peformance.
Technical Support And Services
We provide end-to-end technical support covering documentation, regulatory filing, quality compliance, and in-depth scientific guidance throughout the peptide API lifecycle. From DMF submission and analytical interpretation to customization and post-delivery quality response, our experts ensure reliability, compliance, and smooth program progression.
