EU active substance registration
Swedish Orphan Biovitrum AB (publ)
EU active substance registration SE-H-REG-24-012834 · Sweden
Key facts
| Registration number | SE-H-REG-24-012834 |
|---|---|
| EudraGMDP reference | 49751 |
| Registered site | Swedish Orphan Biovitrum AB (publ) |
| Country | Sweden |
| Competent authority | SE_MPA |
| National site reference | 1727194872666 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 1–9 Third-country API manufacturing sites
- United States Supplier countries outside the EEA
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About EU active substance (API) registrations
Companies in the EEA that manufacture, import or distribute active substances for human medicines must register with their national competent authority. EudraGMDP publishes each registration and the third-country sites that supply the substances.