Suppliers / Bluepharma - Industria Farmaceutica

Bluepharma - Industria Farmaceutica

Portugal 2 duplicate records merged Updated 9 July 2026

Bluepharma - Industria Farmaceutica is a finished-dose manufacturer based in Portugal. It appears in 131 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with INFARMED (PT), EMA and AEMPS (ES). Its GMP standing is certified by INFARMED (PT) and EMA. Its most recent recorded inspection, by US FDA, closed on 13 May 2022 as VAI.

0
active US DMFs
0
valid CEPs
7
registered plants 1 with an FDA FEI number
131
filings across 8 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
6 of 6 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

  • 13 May 2022 VAI US FDA
  • 24 May 2019 VAI US FDA
  • 28 October 2016 VAI US FDA
  • 24 July 2014 NAI US FDA
  • 26 July 2012 VAI US FDA
  • 8 October 2009 NAI US FDA

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

Registered plants

Site FDA FEI
COIMBRA, Portugal Not on file
Coimbra, Portugal Not on file
COIMBRA, Portugal Not on file
Coimbra, Portugal Not on file
Portugal, Portugal 3007007549
Coimbra, Portugal Not on file

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
INFARMED (PT) 63 4
EMA 27 2
AEMPS (ES) 17 None
DAV (Vietnam) 15 None
AIFA (IT) 4 None
MINSA (CR) 2 None

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Open risk flags

  • The most recent inspection outcome was VAI, on 13 May 2022.

Sources on this page

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