Suppliers / Ferrer Internacional

Ferrer Internacional

Spain Updated 9 July 2026

Ferrer Internacional is a finished-dose manufacturer based in Spain. It appears in 440 regulatory filings across 24 regulators, without an active US DMF or CEP on file. Its filings concentrate with AEMPS (ES), EMA and INFARMED (PT). Its GMP standing is certified by AEMPS (ES), TMDA (TZ) and EMA, among 5 authorities.

0
active US DMFs
0
valid CEPs
6
registered plants
440
filings across 24 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
Barcelona, United Arab Emirates Not on file
Barcelona, United Arab Emirates Not on file
SAINT CUGAT DEL VALLÉS, Spain Not on file
Gerona, Spain Not on file
Barcelona, Spain Not on file
Sant Cugat Del Valles, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
AEMPS (ES) 179 3
EMA 53 2
INFARMED (PT) 28 None
MINSA (CR) 28 None
MPA (SE) 22 None
AIFA (IT) 22 None
TMDA (TZ) None 2
NAFDAC (NG) None 1
ANVISA (Brazil) None 1

Questions about Ferrer Internacional

Does Ferrer Internacional hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Ferrer Internacional. It does have 440 filings with 24 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Ferrer Internacional manufacture?
6 registered sites are on record, in United Arab Emirates and Spain (Barcelona, Saint Cugat DEL Vallés and Gerona among others). Every site is listed on this page with the register it came from.
Which regulators recognise Ferrer Internacional's GMP?
Current GMP certificates are on record from AEMPS (ES), TMDA (TZ), EMA, NAFDAC (NG) and ANVISA (Brazil). 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