Suppliers / Qilu Tianhe Pharmaceutical

Qilu Tianhe Pharmaceutical

China Updated 9 July 2026

The public registers hold a second record for Qilu Tianhe Pharmaceutical. The fuller profile, with 31 active US DMFs and 12 valid CEPs, is at Qilu Pharmaceutical. Figures on this page cover only this record.

Qilu Tianhe Pharmaceutical is an API manufacturer based in China. Its GMP standing is certified by MHRA (UK).

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

Registered plants

Site FDA FEI
SHANDONG, China Not on file
JINAN, China Not on file

What they file, and where

Molecule Regulators Docs
Amikacin SFDA (Saudi Arabia) 1
Hydroxyurea SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Amikacin API Hydroxyurea API

Filings and GMP by regulator

Regulator Filings GMP certificates
MHRA (UK) None 2

Questions about Qilu Tianhe Pharmaceutical

Where does Qilu Tianhe Pharmaceutical manufacture?
2 registered sites are on record, in China (Shandong and Jinan). Every site is listed on this page with the register it came from.
What does Qilu Tianhe Pharmaceutical make?
2 molecules are on record against Qilu Tianhe Pharmaceutical, including Amikacin and Hydroxyurea. Each links through to that molecule's full manufacturer list.
Which regulators recognise Qilu Tianhe Pharmaceutical's GMP?
Current GMP certificates are on record from MHRA (UK). 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