Suppliers / Boehringer Ingelheim Do Brasil Quimica E Farmaceutica Ltda

Boehringer Ingelheim Do Brasil Quimica E Farmaceutica Ltda

Brazil Updated 9 July 2026

Boehringer Ingelheim Do Brasil Quimica E Farmaceutica Ltda is a finished-dose manufacturer based in Brazil. It appears in 176 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil), INVIMA (CO) and ARCSA (EC). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
4
registered plants
176
filings across 3 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
ITAPECERICA DA SERRA, Brazil Not on file
São Paulo, Brazil Not on file
SAO PAULO, Brazil Not on file
Itapecerica da Serra - Sao Paulo, SP, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 172 None
INVIMA (CO) 3 None
ARCSA (EC) 1 None
EMA None 1

Questions about Boehringer Ingelheim Do Brasil Quimica E Farmaceutica Ltda

Does Boehringer Ingelheim Do Brasil Quimica E Farmaceutica Ltda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Boehringer Ingelheim Do Brasil Quimica E Farmaceutica Ltda. It does have 176 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Boehringer Ingelheim Do Brasil Quimica E Farmaceutica Ltda manufacture?
4 registered sites are on record, in Brazil (Itapecerica DA Serra, São Paulo and SAO Paulo among others). Every site is listed on this page with the register it came from.
Which regulators recognise Boehringer Ingelheim Do Brasil Quimica E Farmaceutica Ltda's GMP?
Current GMP certificates are on record from 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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Sources on this page

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