Suppliers / Laboratorio Globo

Laboratorio Globo

Brazil 15 employees Updated 9 July 2026

Laboratorio Globo is a finished-dose manufacturer based in Brazil. It appears in 413 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
1
registered plants
413
filings across 1 regulators

Registered plants

Site FDA FEI
SAO JOSE DA LAPA, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 413 3

Questions about Laboratorio Globo

Does Laboratorio Globo hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Globo. It does have 413 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Globo manufacture?
1 registered site is on record, in Brazil (SAO Jose DA Lapa). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Globo'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