Suppliers / Tianjin Tasly Sants Pharmaceutical

Tianjin Tasly Sants Pharmaceutical

China Updated 9 July 2026

Tianjin Tasly Sants Pharmaceutical is an API manufacturer based in China. It holds one active US drug master file. Its GMP standing is certified by EMA and MHRA (UK).

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

Registered plants

Site FDA FEI
TIANJIN, China Not on file

What they file, and where

Molecule Regulators Docs
Eszopiclone US FDA 1

Also appears on these molecule pages

Eszopiclone API

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1
MHRA (UK) None 1

Questions about Tianjin Tasly Sants Pharmaceutical

Does Tianjin Tasly Sants Pharmaceutical hold a US DMF or a CEP?
Tianjin Tasly Sants Pharmaceutical holds 1 active US drug master file. 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 Tianjin Tasly Sants Pharmaceutical manufacture?
1 registered site is on record, in China (Tianjin). Every site is listed on this page with the register it came from.
What does Tianjin Tasly Sants Pharmaceutical make?
1 molecule is on record against Tianjin Tasly Sants Pharmaceutical, including Eszopiclone. Each links through to that molecule's full manufacturer list.
Which regulators recognise Tianjin Tasly Sants Pharmaceutical's GMP?
Current GMP certificates are on record from EMA and 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