Suppliers / Lecifarma - Laboratório Farmacêutico, Lda

Lecifarma - Laboratório Farmacêutico, Lda

Portugal 45 employees Updated 9 July 2026

Lecifarma - Laboratório Farmacêutico, Lda is a finished-dose manufacturer based in Portugal. It appears in 7 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with INFARMED (PT), EEC_EAEU and JFDA (JO). Its GMP standing is certified by INFARMED (PT).

0
active US DMFs
0
valid CEPs
4
registered plants
7
filings across 4 regulators

Registered plants

Site FDA FEI
Loures, United Arab Emirates Not on file
LOUSÃ LOURES, Portugal Not on file
Loures, Portugal Not on file
Loures, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INFARMED (PT) 3 2
EEC_EAEU 2 None
JFDA (JO) 1 None
EDE (AE) 1 None

Questions about Lecifarma - Laboratório Farmacêutico, Lda

Does Lecifarma - Laboratório Farmacêutico, Lda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Lecifarma - Laboratório Farmacêutico, Lda. It does have 7 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Lecifarma - Laboratório Farmacêutico, Lda manufacture?
4 registered sites are on record, in United Arab Emirates and Portugal (Loures and Lousã Loures among others). Every site is listed on this page with the register it came from.
Which regulators recognise Lecifarma - Laboratório Farmacêutico, Lda's GMP?
Current GMP certificates are on record from INFARMED (PT). 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