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.
| 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.
| 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 |
| 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 We do not publish the identity of any buyer.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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