Suppliers / Pierre Fabre Pharmaceuticals

Pierre Fabre Pharmaceuticals

France Updated 9 July 2026

Pierre Fabre Pharmaceuticals is a finished-dose manufacturer based in France. It appears in 90 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with SWISSMEDIC (CH), AIFA (IT) and EMA. Its GMP standing is certified by ZLG (DE) and EMA.

0
active US DMFs
0
valid CEPs
6
registered plants 1 with an FDA FEI number
90
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Palezieux, Switzerland Not on file
Basel, Switzerland Not on file
Freiburg Im Breisgau, Germany Not on file
Baden-Wuerttemberg, Germany Not on file
Freiburg, Germany Not on file
Aurora, United States 3038219610

Filings and GMP by regulator

Regulator Filings GMP certificates
SWISSMEDIC (CH) 68 None
AIFA (IT) 14 None
EMA 8 3
ZLG (DE) None 8

Questions about Pierre Fabre Pharmaceuticals

Does Pierre Fabre Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pierre Fabre Pharmaceuticals. It does have 90 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Pierre Fabre Pharmaceuticals FDA-registered?
One site operated by Pierre Fabre Pharmaceuticals carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Pierre Fabre Pharmaceuticals manufacture?
6 registered sites are on record, in Switzerland, Germany and United States (Palezieux, Basel and Freiburg Im Breisgau among others). Every site is listed on this page with the register it came from.
Which regulators recognise Pierre Fabre Pharmaceuticals's GMP?
Current GMP certificates are on record from ZLG (DE) 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