Leo Pharm is a finished-dose manufacturer based in Denmark. It appears in 17 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDA (EG) and US FDA.
| Regulator | Filings | GMP certificates |
|---|---|---|
| EDA (EG) | 14 | None |
| US FDA | 3 | None |
Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.
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