Suppliers / Laboratórios Atral

Laboratórios Atral

Portugal 222 employees 2 duplicate records merged Updated 9 July 2026

Laboratórios Atral is a finished-dose manufacturer based in Portugal. It appears in 400 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with INFARMED (PT), EMA and INVIMA (CO). Its GMP standing is certified by INFARMED (PT).

0
active US DMFs
0
valid CEPs
6
registered plants 1 with an FDA FEI number
400
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Montijo, Portugal Not on file
Castanhera do Ribatejo, Portugal Not on file
Alverca de Ribatejo, Portugal Not on file
Castanheira do Ribatejo, Portugal Not on file
Portugal, Portugal 3002806420
Montijo, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INFARMED (PT) 329 2
EMA 69 None
INVIMA (CO) 2 None

Questions about Laboratórios Atral

Does Laboratórios Atral hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratórios Atral. It does have 400 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Laboratórios Atral FDA-registered?
One site operated by Laboratórios Atral carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Laboratórios Atral manufacture?
6 registered sites are on record, in Portugal (Montijo, Castanhera Do Ribatejo and Alverca De Ribatejo among others). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratórios Atral'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