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), MINSA (CR) and EMA. 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
Póvoa de Sto. Adrião, Portugal Not on file
Barcarena, Portugal Not on file
Barcarena, Portugal Not on file
Portugal, Portugal 3032992682

6 further sites are on record.

Filings and GMP by regulator

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

Questions about Lusomedicamenta Sociedade Técnica Farmacêutica

Does Lusomedicamenta Sociedade Técnica Farmacêutica hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Lusomedicamenta Sociedade Técnica Farmacêutica. It does have 7 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Lusomedicamenta Sociedade Técnica Farmacêutica FDA-registered?
2 sites operated by Lusomedicamenta Sociedade Técnica Farmacêutica carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Lusomedicamenta Sociedade Técnica Farmacêutica's last inspection go?
The most recent inspection on record closed on 18 October 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 2 inspections are on file.
Where does Lusomedicamenta Sociedade Técnica Farmacêutica manufacture?
12 registered sites are on record, in United Arab Emirates and Portugal (Barcarena, Portugal and Póvoa De Sto. Adrião among others). Every site is listed on this page with the register it came from.
Which regulators recognise Lusomedicamenta Sociedade Técnica Farmacêutica's GMP?
Current GMP certificates are on record from EMA, INFARMED (PT), ANVISA (Brazil) and US FDA. 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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  • The most recent inspection outcome was VAI, on 18 October 2024.

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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