Suppliers / Shandong Kexing Bioproducts

Shandong Kexing Bioproducts

China Updated 9 July 2026

Shandong Kexing Bioproducts is a finished-dose manufacturer based in China. It appears in 10 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), EDA (EG) and BOMRA (BW). Its GMP standing is certified by UZPHARM (UZ) and EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
10
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
0 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Jinan, China Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 4 None
EDA (EG) 2 None
BOMRA (BW) 1 None
UZPHARM (UZ) 1 1
NAFDAC (NG) 1 None
DIGEMAPS (DO) 1 None
EMA None 1

Questions about Shandong Kexing Bioproducts

Does Shandong Kexing Bioproducts hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Shandong Kexing Bioproducts. It does have 10 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Shandong Kexing Bioproducts manufacture?
1 registered site is on record, in China (Jinan). Every site is listed on this page with the register it came from.
Which regulators recognise Shandong Kexing Bioproducts's GMP?
Current GMP certificates are on record from UZPHARM (UZ) and EMA. 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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates