Suppliers / Laboratorio Gross S A

Laboratorio Gross S A

Brazil 45 employees Updated 9 July 2026

Laboratorio Gross S A is a finished-dose manufacturer based in Brazil. It appears in 73 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
73
filings across 1 regulators

Registered plants

Site FDA FEI
RIO DE JANEIRO, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 73 3

Questions about Laboratorio Gross S A

Does Laboratorio Gross S A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Gross S A. It does have 73 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Gross S A manufacture?
1 registered site is on record, in Brazil (RIO DE Janeiro). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Gross S A'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