Mundipharma is a finished-dose manufacturer based in Germany. It appears in 952 regulatory filings across 23 regulators, without an active US DMF or CEP on file. Its filings concentrate with AIFA (IT), EMA and MPA (SE). Its GMP standing is certified by HSA (SG), EMA and ZLG (DE), among 4 authorities.
| Site | FDA FEI |
|---|---|
| Nicosia, United Arab Emirates | Not on file |
| Basel, Switzerland | Not on file |
| Basel, Switzerland | Not on file |
| Nicosia, Cyprus | Not on file |
| LIMBURG AN DER LAHN, Germany | Not on file |
| Hessen, Germany | Not on file |
2 further sites are on record.
| Regulator | Filings | GMP certificates |
|---|---|---|
| AIFA (IT) | 165 | None |
| EMA | 113 | 2 |
| MPA (SE) | 98 | None |
| SWISSMEDIC (CH) | 69 | None |
| MEDSAFE (NZ) | 67 | None |
| SAHPRA (ZA) | 63 | None |
| HSA (SG) | None | 5 |
| ZLG (DE) | None | 2 |
| MFDS (Korea) | None | 2 |
Choose your molecules and target markets. Mundipharma comes back tiered against every other supplier able to file there.
Start for free