Suppliers / Kunming Guiyan Pharmaceutical

Kunming Guiyan Pharmaceutical

China Updated 9 July 2026

Kunming Guiyan Pharmaceutical is an API manufacturer based in China. It holds 4 active US drug master files and 3 valid CEPs across a filed portfolio of 3 molecules.

4
active US DMFs
3
valid CEPs
1
registered plants
1
filings across 1 regulators

Registered plants

Site FDA FEI
Kunming, China Not on file

What they file, and where

Molecule Regulators Docs
Carboplatin EDQM, US FDA 3
Oxaliplatin EDQM, US FDA 3
Cisplatin EDQM 1

Also appears on these molecule pages

Carboplatin API Cisplatin API Oxaliplatin API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None

Questions about Kunming Guiyan Pharmaceutical

Does Kunming Guiyan Pharmaceutical hold a US DMF or a CEP?
Kunming Guiyan Pharmaceutical holds 4 active US drug master files and 3 valid CEPs. 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.
Where does Kunming Guiyan Pharmaceutical manufacture?
1 registered site is on record, in China (Kunming). Every site is listed on this page with the register it came from.
What does Kunming Guiyan Pharmaceutical make?
3 molecules are on record against Kunming Guiyan Pharmaceutical, including Carboplatin, Oxaliplatin and Cisplatin. Each links through to that molecule's full manufacturer list.
Where does Kunming Guiyan Pharmaceutical file?
Filings are on record with MINSA (CR), 1 in total.

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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Sources on this page

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