Vifor (International) is an API and finished-dose manufacturer based in Switzerland. It appears in 196 regulatory filings across 24 regulators, without an active US DMF or CEP on file. Its filings concentrate with SWISSMEDIC (CH), EMA and DIGEMAPS (DO). Its GMP standing is certified by ANSM (FR), EMA and ANVISA (Brazil), among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 6 September 2024 as VAI.
NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.
| Site | FDA FEI |
|---|---|
| St. Gallen, United Arab Emirates | Not on file |
| 92042 PARIS LA DEFENSE, United Arab Emirates | Not on file |
| ST. GALLEN, Switzerland | Not on file |
| Saint Gall, Switzerland | Not on file |
| Switzerland, Switzerland | 3002808450 |
| Paris La Defense Cedex, France | Not on file |
1 further sites are on record.
| Molecule | Regulators | Docs |
|---|---|---|
| Ferric Carboxymaltose | SFDA (Saudi Arabia) | 1 |
| Iron Sucrose | PMDA (Japan) | 1 |
| カルボキシマルトース第二鉄 | PMDA (Japan) | 1 |
Also appears on these molecule pages
| Regulator | Filings | GMP certificates |
|---|---|---|
| SWISSMEDIC (CH) | 59 | None |
| EMA | 23 | 3 |
| DIGEMAPS (DO) | 13 | None |
| AIFA (IT) | 12 | None |
| UZPHARM (UZ) | 10 | None |
| INFARMED (PT) | 9 | None |
| ANSM (FR) | None | 3 |
| ANVISA (Brazil) | None | 1 |
| US FDA | None | 1 |
Choose your molecules and target markets. Vifor (International) comes back tiered against every other supplier able to file there.
Start for free