Suppliers / Lusomedicamenta Sociedade Técnica Farmacêutica

Lusomedicamenta Sociedade Técnica Farmacêutica

Portugal Updated 9 July 2026

Lusomedicamenta Sociedade Técnica Farmacêutica is a finished-dose manufacturer based in Portugal. It appears in 7 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with INFARMED (PT), EMA and MINSA (CR). Its GMP standing is certified by EMA, INFARMED (PT) and ANVISA (Brazil), among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 18 October 2024 as VAI.

0
active US DMFs
0
valid CEPs
12
registered plants 2 with an FDA FEI number
7
filings across 3 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

  • 18 October 2024 VAI US FDA
  • 27 September 2019 VAI US FDA

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

Registered plants

Site FDA FEI
Barcarena, United Arab Emirates Not on file
Portugal, Portugal 3005491771
Barcarena, Portugal Not on file
Póvoa de Sto. Adrião, Portugal Not on file
Portugal, Portugal 3032992682
Póvoa Sto. Adrião, Portugal Not on file

6 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
INFARMED (PT) 5 2
EMA 1 4
MINSA (CR) 1 None
ANVISA (Brazil) None 2
US FDA None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 18 October 2024.

Sources on this page

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