Suppliers / Pharlab Industria Farmaceutica

Pharlab Industria Farmaceutica

Brazil 763 employees Updated 9 July 2026

Pharlab Industria Farmaceutica is a finished-dose manufacturer based in Brazil. It appears in 405 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil) and NAFDAC (NG). Its GMP standing is certified by ANVISA (Brazil), EMA and NAFDAC (NG).

0
active US DMFs
0
valid CEPs
1
registered plants
405
filings across 2 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
LAGOA DA PRATA, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 402 2
NAFDAC (NG) 3 1
EMA None 2

Questions about Pharlab Industria Farmaceutica

Does Pharlab Industria Farmaceutica hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pharlab Industria Farmaceutica. It does have 405 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Pharlab Industria Farmaceutica manufacture?
1 registered site is on record, in Brazil (Lagoa DA Prata). Every site is listed on this page with the register it came from.
Which regulators recognise Pharlab Industria Farmaceutica's GMP?
Current GMP certificates are on record from ANVISA (Brazil), EMA and NAFDAC (NG). 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