Suppliers / Laboratório Edol - Produtos Farmacêuticos

Laboratório Edol - Produtos Farmacêuticos

Portugal 211 employees Updated 9 July 2026

Laboratório Edol - Produtos Farmacêuticos is a finished-dose manufacturer based in Portugal. It appears in 175 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with INFARMED (PT), EMA and RAMA (GE). Its GMP standing is certified by INFARMED (PT) and EMA.

0
active US DMFs
0
valid CEPs
5
registered plants
175
filings across 4 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Carnaxide, Portugal Not on file
Carnaxide, Portugal Not on file
Montijo, Portugal Not on file
Linda-a-Velha, Portugal Not on file
Carnaxide, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INFARMED (PT) 113 6
EMA 58 1
RAMA (GE) 2 None
JFDA (JO) 2 None

Questions about Laboratório Edol - Produtos Farmacêuticos

Does Laboratório Edol - Produtos Farmacêuticos hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratório Edol - Produtos Farmacêuticos. It does have 175 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratório Edol - Produtos Farmacêuticos manufacture?
5 registered sites are on record, in Portugal (Carnaxide, Montijo and Linda-a-velha among others). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratório Edol - Produtos Farmacêuticos's GMP?
Current GMP certificates are on record from INFARMED (PT) and EMA. 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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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