Suppliers / Industrial Farmacéutica Cantabria

Industrial Farmacéutica Cantabria

Spain 5 employees Updated 9 July 2026

Industrial Farmacéutica Cantabria is a finished-dose manufacturer based in Spain. It appears in 197 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), AEMPS (ES) and EMA. Its GMP standing is certified by AEMPS (ES), US FDA and EAEU_EEC, among 5 authorities. Its most recent recorded inspection, by US FDA, closed on 17 May 2024 as VAI.

0
active US DMFs
0
valid CEPs
7
registered plants 2 with an FDA FEI number
197
filings across 9 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
2 of 2 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 17 May 2024 VAI US FDA
  • 6 September 2023 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Santander, United Arab Emirates Not on file
Madrid, Spain Not on file
Cantabria, Spain Not on file
SANTANDER, Spain Not on file
Torrejon De Ardoz, Spain Not on file
Spain, Spain 3005887891

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 103 None
AEMPS (ES) 56 3
EMA 29 1
NPRA (MY) 3 None
EDE (AE) 2 None
MPA (SE) 1 None
US FDA None 2
EAEU_EEC None 1
ANVISA (Brazil) None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 17 May 2024.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates