Orion is a finished-dose manufacturer based in Finland. It appears in 2,474 regulatory filings across 27 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, MPA (SE) and DKMA (DK). Its GMP standing is certified by MFDS (Korea), ANVISA (Brazil) and NCELS (KZ), among 6 authorities.
| Site | FDA FEI |
|---|---|
| Espoo, United Arab Emirates | Not on file |
| Salo, United Arab Emirates | Not on file |
| Zug, Switzerland | Not on file |
| SALO, Finland | Not on file |
| Fermion Espoo, Finland | Not on file |
| Regulator | Filings | GMP certificates |
|---|---|---|
| EMA | 712 | 1 |
| MPA (SE) | 628 | None |
| DKMA (DK) | 291 | None |
| AIFA (IT) | 181 | None |
| FAMHP (BE) | 152 | None |
| DMP (NO) | 95 | None |
| MFDS (Korea) | None | 4 |
| ANVISA (Brazil) | None | 4 |
| NCELS (KZ) | None | 3 |
| EAEU_EEC | None | 2 |
| HSA (SG) | None | 2 |
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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