Suppliers / Chiesi Farmaceutica Ltda

Chiesi Farmaceutica Ltda

Brazil 11 employees Updated 9 July 2026

Chiesi Farmaceutica Ltda is a finished-dose manufacturer based in Brazil. It appears in 137 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANVISA (Brazil) and US FDA. Its GMP standing is certified by ANVISA (Brazil) and EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
137
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
SANTANA DE PARNAIBA, Brazil Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) 131 5
US FDA 6 None
EMA None 1

Questions about Chiesi Farmaceutica Ltda

Does Chiesi Farmaceutica Ltda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Chiesi Farmaceutica Ltda. It does have 137 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Chiesi Farmaceutica Ltda manufacture?
1 registered site is on record, in Brazil (Santana DE Parnaiba). Every site is listed on this page with the register it came from.
Which regulators recognise Chiesi Farmaceutica Ltda's GMP?
Current GMP certificates are on record from ANVISA (Brazil) and 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