Suppliers / Laboratorio Quimico Farmacéutico Bergamo Ltda

Laboratorio Quimico Farmacéutico Bergamo Ltda

Brazil Updated 9 July 2026

Laboratorio Quimico Farmacéutico Bergamo Ltda is a finished-dose manufacturer based in Brazil. It appears in 293 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil) and ARCSA (EC). Its GMP standing is certified by ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
3
registered plants
293
filings across 2 regulators

Registered plants

Site FDA FEI
TABOAO DA SERRA, Brazil Not on file
COTIA, Brazil Not on file
Taboao Da Serra, Colombia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 288 5
ARCSA (EC) 5 None

Questions about Laboratorio Quimico Farmacéutico Bergamo Ltda

Does Laboratorio Quimico Farmacéutico Bergamo Ltda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Quimico Farmacéutico Bergamo Ltda. It does have 293 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Quimico Farmacéutico Bergamo Ltda manufacture?
3 registered sites are on record, in Brazil and Colombia (Taboao DA Serra, Cotia and Taboao Da Serra). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Quimico Farmacéutico Bergamo Ltda'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