Suppliers / Qingdao Kingway Pharmatech

Qingdao Kingway Pharmatech

China Updated 9 July 2026

Qingdao Kingway Pharmatech is an API and finished-dose manufacturer based in China. It appears in 96 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with EEC_EAEU, HSA (SG) and ISP (CL). Its GMP standing is certified by HSA (SG).

0
active US DMFs
0
valid CEPs
2
registered plants
96
filings across 9 regulators

Registered plants

Site FDA FEI
Las Vegas, United Arab Emirates Not on file
BENSLIMANE, Morocco Not on file

What they file, and where

Molecule Regulators Docs
Bisoprolol SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Bisoprolol API Glipizide finished dose Omega-3 Fatty Acids finished dose

Filings and GMP by regulator

Regulator Filings GMP certificates
EEC_EAEU 48 None
HSA (SG) 24 2
ISP (CL) 12 None
DMP (NO) 6 None
EDE (AE) 2 None
MINSA (CR) 1 None

Questions about Qingdao Kingway Pharmatech

Does Qingdao Kingway Pharmatech hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Qingdao Kingway Pharmatech. It does have 96 filings with 9 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Qingdao Kingway Pharmatech manufacture?
2 registered sites are on record, in United Arab Emirates and Morocco (Las Vegas and Benslimane). Every site is listed on this page with the register it came from.
What does Qingdao Kingway Pharmatech make?
1 molecule is on record against Qingdao Kingway Pharmatech, including Bisoprolol. Each links through to that molecule's full manufacturer list.
Which regulators recognise Qingdao Kingway Pharmatech's GMP?
Current GMP certificates are on record from HSA (SG). 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