Suppliers / Cisen Pharmaceutical

Cisen Pharmaceutical

China 35 employees 3 duplicate records merged Updated 9 July 2026

Cisen Pharmaceutical is a finished-dose manufacturer based in China. It appears in 80 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), UZPHARM (UZ) and MINSA (CR). Its GMP standing is certified by UZPHARM (UZ), NAFDAC (NG) and MCAZ (ZW).

0
active US DMFs
0
valid CEPs
1
registered plants
80
filings across 6 regulators

Registered plants

Site FDA FEI
P.R. China, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 29 None
UZPHARM (UZ) 23 4
MINSA (CR) 13 None
DIGEMAPS (DO) 10 None
NAFDAC (NG) 3 2
US FDA 2 None
MCAZ (ZW) None 1

Questions about Cisen Pharmaceutical

Does Cisen Pharmaceutical hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Cisen Pharmaceutical. It does have 80 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Cisen Pharmaceutical manufacture?
1 registered site is on record, in Nigeria (P.r. China). Every site is listed on this page with the register it came from.
Which regulators recognise Cisen Pharmaceutical's GMP?
Current GMP certificates are on record from UZPHARM (UZ), NAFDAC (NG) and MCAZ (ZW). 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