Suppliers / Atlantic Pharma - Producoes Farmaceuticas

Atlantic Pharma - Producoes Farmaceuticas

Portugal 2 duplicate records merged Updated 9 July 2026

Atlantic Pharma - Producoes Farmaceuticas is a finished-dose manufacturer based in Portugal. It appears in 149 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with EEC_EAEU, NPRA (MY) and ARCSA (EC). Its GMP standing is certified by ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
4
registered plants
149
filings across 10 regulators

Registered plants

Site FDA FEI
Sintra, United Arab Emirates Not on file
Sintra, United Arab Emirates Not on file
Porto, Portugal Not on file
SINTRA, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EEC_EAEU 49 None
NPRA (MY) 27 None
ARCSA (EC) 25 None
INVIMA (CO) 20 None
MINSA (CR) 9 None
DIGEMAPS (DO) 5 None
ANVISA (Brazil) None 9

Questions about Atlantic Pharma - Producoes Farmaceuticas

Does Atlantic Pharma - Producoes Farmaceuticas hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Atlantic Pharma - Producoes Farmaceuticas. It does have 149 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Atlantic Pharma - Producoes Farmaceuticas manufacture?
4 registered sites are on record, in United Arab Emirates and Portugal (Sintra, Porto and Sintra among others). Every site is listed on this page with the register it came from.
Which regulators recognise Atlantic Pharma - Producoes Farmaceuticas's GMP?
Current GMP certificates are on record from ANVISA (Brazil). 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