Suppliers / Pierre Fabre Medicament Production

Pierre Fabre Medicament Production

France 176 employees Updated 9 July 2026

Pierre Fabre Medicament Production is a finished-dose manufacturer based in France. It appears in 78 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with DPM (TN), EDE (AE) and MINSA (CR). Its GMP standing is certified by ANSM (FR), EMA and NAFDAC (NG), among 5 authorities.

0
active US DMFs
0
valid CEPs
10
registered plants 1 with an FDA FEI number
78
filings across 8 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
Cahors, United Arab Emirates Not on file
Gien Cedex, United Arab Emirates Not on file
Gien, United Arab Emirates Not on file
GIEN, France Not on file
France, France 3006185766
Cahors, France Not on file

4 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
DPM (TN) 34 None
EDE (AE) 12 None
MINSA (CR) 10 None
UZPHARM (UZ) 9 None
EEC_EAEU 5 None
DIGEMAPS (DO) 4 None
ANSM (FR) None 14
EMA None 4
NAFDAC (NG) None 1
ANVISA (Brazil) None 1
EAEU_EEC None 1

Scale

Year Revenue Exports Destinations
2024 $0 Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

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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
Company filings
Revenue as reported