Suppliers / Laboratorios Cinfa S A

Laboratorios Cinfa S A

Spain Updated 9 July 2026

Laboratorios Cinfa S A is a finished-dose manufacturer based in Spain. It appears in 1,256 regulatory filings across 11 regulators, without an active US DMF or CEP on file. Its filings concentrate with AEMPS (ES), EMA and SFDA (Saudi Arabia). Its GMP standing is certified by AEMPS (ES), EMA and EAEU_EEC.

0
active US DMFs
0
valid CEPs
6
registered plants
1,256
filings across 11 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
Navarre, United Arab Emirates Not on file
Areta Huarte, United Arab Emirates Not on file
Olloki, United Arab Emirates Not on file
Madrid, Spain Not on file
Navarra, Spain Not on file
Huarte, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
AEMPS (ES) 799 3
EMA 358 1
SFDA (Saudi Arabia) 57 None
DIGEMAPS (DO) 12 None
MINSA (CR) 10 None
MPA (SE) 7 None
EAEU_EEC None 1

Questions about Laboratorios Cinfa S A

Does Laboratorios Cinfa S A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Cinfa S A. It does have 1,256 filings with 11 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Cinfa S A manufacture?
6 registered sites are on record, in United Arab Emirates and Spain (Navarre, Areta Huarte and Olloki among others). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Cinfa S A's GMP?
Current GMP certificates are on record from AEMPS (ES), EMA and EEC (Eurasian Economic Union). 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