Suppliers / Guizhou Utide Biotechnology

Guizhou Utide Biotechnology

China Updated 9 July 2026

Guizhou Utide Biotechnology is a contract manufacturer based in China. It holds 2 active US drug master files across a filed portfolio of 2 molecules.

2
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Retatrutide US FDA 1
Tirzepatide US FDA 1

Also appears on these molecule pages

Retatrutide contract manufacturing Semaglutide contract manufacturing Tirzepatide contract manufacturing

Questions about Guizhou Utide Biotechnology

Does Guizhou Utide Biotechnology hold a US DMF or a CEP?
Guizhou Utide Biotechnology holds 2 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
What does Guizhou Utide Biotechnology make?
2 molecules are on record against Guizhou Utide Biotechnology, including Retatrutide and Tirzepatide. Each links through to that molecule's full manufacturer list.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability