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Brochure & Flyers

Utide Brochure
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.
Flyers
These one-page flyers provide a concise yet comprehensive introduction to UTIDE’s core capabilities, product strengths, and quality standards.
Each customized peptide is accompanied by a detailed Certificate of Analysis (COA), providing full transparency into critical quality attributes.
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.
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.