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UTIDE BIOTECH (SHENZHEN)CO., LIMITED

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会社概要

  • 正式社名: UTIDE BIOTECH (SHENZHEN)CO., LIMITED
  • 国際名称: 优泰生物 (Utide Biotech (Shenzhen) Co., Limited), Shenzhen, Guangdong, China, of 贵州优泰生物科技有限公司 (Guizhou Utide Biotechnology Co., Ltd.), Zunyi, Guizhou
  • ブランド名 / 商号: Utide
  • 登録国: China
  • 住所: Guangdong
説明:

Utide is a specialized manufacturer of GLP-1 peptide APIs, operating 20,000 square meters of manufacturing space in Zunyi, Guizhou, China. Backed by a core team with more than 20 years of experience in peptide R&D, process development and GMP-oriented manufacturing, Utide holds strong capabilities in route development, process optimization and rapid scale-up across a wide range of high-demand peptide products. With its Phase II facility now online, total annual production capacity is expected to reach 1,500-1,800 kg this year, supporting reliable, scalable long-term supply. The company has secured U.S. FDA Drug Master Files for tirzepatide (DMF No. 042984) and retatrutide (DMF No. 043330), with further global regulatory filings underway. Melos serves as Utide's exclusive strategic partner and commercial entity for Southeast and South Asia, acting as the core platform for Utide's international business development in those markets. Backed by a team with extensive international business and supply chain experience, Melos specializes in providing professional supply solutions and integrated commercial support for GLP-1 peptide APIs, handling regional contract execution, payment settlement, logistics coordination and customer support to ensure smooth, reliable and compliant delivery of Utide's peptide APIs throughout the region.

事業活動

受託・アウトソーシングサービス

医薬品開発製造受託機関(CDMO)

バイオ医薬品

バイオテクノロジー・バイオ医薬品企業

原薬(API)

原薬メーカー
販売市場

当社の製品・サービス

認証

ISO 90001

ISO 1400

ISO 45001:2018

GMP-oriented manufacturing

FDA Drug Master Files

DMFs

DMF NO

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