Suppliers / Ems S/A

Ems S/A

Brazil Updated 9 July 2026

Ems S/A is a finished-dose manufacturer based in Brazil. It appears in 2,623 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil), ARCSA (EC) and MINSA (CR). Its GMP standing is certified by ANVISA (Brazil) and EMA.

0
active US DMFs
0
valid CEPs
3
registered plants
2,623
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
SANTA MARIA, Brazil Not on file
HORTOLANDIA, Brazil Not on file
SÃO BERNARDO DO CAMPO, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 2,576 8
ARCSA (EC) 39 None
MINSA (CR) 4 None
DIGEMAPS (DO) 4 None
EMA None 1

Scale

Year Revenue Exports Destinations
2024 $430K Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Comparing suppliers?

Choose your molecules and target markets. Ems S/A comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Company filings
Revenue as reported