Brochure & Flyers
Comprehensive Product Documentation & Quality Certificates
for UTIDE Custom Peptides
Utide Brochure
Company Overview
This brochure provides a comprehensive overview of Guizhou Utide Biotechnology Co., Ltd., documenting our specialized manufacturing capabilities, regulatory achievements, and commitment to delivering high-purity peptide APIs for global partners.
Guizhou Utide Biotechnology Co., Ltd., headquartered in Zunyi, Guizhou Province, is a specialized manufacturer of GLP-1 peptide active pharmaceutical ingredients (APIs), with 20,000 square meters of manufacturing facilities.
Our core team has over 20 years of experience in peptide research and development and GMP-compliant manufacturing, with strong expertise in synthetic route development, process optimization, and rapid scale-up. Phase I and Phase II production facilities are fully operational, and a Phase III GMP manufacturing facility is planned for expansion.
We have successfully obtained U.S. Drug Master Files (DMFs) for tirzepatide (DMF No. 042984) and retatrutide (DMF No. 043330), with additional regulatory filings in progress globally.
Supported by dedicated teams in Guizhou, Shenzhen, and Hong Kong, Utide provides high-purity custom peptide APIs and tailored development solutions to partners worldwide.
Product Flyers
Quality Documentation
These one-page flyers provide a concise yet comprehensive introduction to UTIDE’s core capabilities, product strengths, and quality standards, documenting the rigorous quality control processes applied to our peptide APIs.
Each customized peptide is accompanied by a detailed Certificate of Analysis (COA), providing full transparency into critical quality attributes including purity, impurities, and batch consistency data.
Our peptides are manufactured under stringent quality control processes and are characterized by high purity (≥99% by UPLC), low impurity profiles, controlled residual solvent levels, and excellent batch-to-batch consistency, ensuring suitability for demanding research and preclinical applications.
All documentation is prepared in accordance with international quality standards and regulatory requirements, ensuring compliance and traceability throughout the product lifecycle.
Through clear, data-driven COA documentation, UTIDE enables customers to rapidly assess product quality, regulatory compliance, and application readiness, supporting confident product selection and efficient project advancement.