Suppliers / Beijing Jincheng Taier Pharmaceutical

Beijing Jincheng Taier Pharmaceutical

China Updated 9 July 2026

Beijing Jincheng Taier Pharmaceutical is an API manufacturer based in China. It holds 3 valid CEPs across a filed portfolio of 3 molecules. Its GMP standing is certified by MFDS (Korea).

0
active US DMFs
3
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Beiwu Town, China Not on file

What they file, and where

Molecule Regulators Docs
Bisoprolol EDQM 1
Mefenamic Acid EDQM 1
Oseltamivir EDQM 1

Also appears on these molecule pages

Bisoprolol API Mefenamic Acid API Oseltamivir API

Filings and GMP by regulator

Regulator Filings GMP certificates
MFDS (Korea) None 2

Questions about Beijing Jincheng Taier Pharmaceutical

Does Beijing Jincheng Taier Pharmaceutical hold a US DMF or a CEP?
Beijing Jincheng Taier Pharmaceutical holds 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 Beijing Jincheng Taier Pharmaceutical manufacture?
1 registered site is on record, in China (Beiwu Town). Every site is listed on this page with the register it came from.
What does Beijing Jincheng Taier Pharmaceutical make?
3 molecules are on record against Beijing Jincheng Taier Pharmaceutical, including Bisoprolol, Mefenamic Acid and Oseltamivir. Each links through to that molecule's full manufacturer list.
Which regulators recognise Beijing Jincheng Taier Pharmaceutical's GMP?
Current GMP certificates are on record from MFDS (Korea). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates