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 | 48800 |
| Registration holder | Swedish Orphan Biovitrum AB (publ) |
| Registered site | Swedish Orphan Biovitrum AB (publ) |
| Site address | Strandbergsgatan 49, Vastermalm, Stockholm, 112 51 |
| Country | Sweden |
| Competent authority | SE_MPA |
| National site reference | 122931343640172606 |
| OMS location ID | LOC-100007941 |
| OMS organisation ID | ORG-100000672 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- None Third-country API manufacturing sites
- 1–9 EudraGMDP certificates and reports for this site
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.