EU active substance registration
Cytomed Oy
EU active substance registration 2442/11.01.01/2013/FIN-9 · Finland
Key facts
| Registration number | 2442/11.01.01/2013/FIN-9 |
|---|---|
| EudraGMDP reference | 42012 |
| Registration holder | Cytomed Oy |
| Registered site | Cytomed Oy |
| Site address | Laastitie 1, Rauha, FI-55300 |
| Country | Finland |
| Competent authority | FI_FIMEA |
| National site reference | 177491377677112493 |
| OMS location ID | LOC-100028394 |
| OMS organisation ID | ORG-100019636 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 1–9 Third-country API manufacturing sites
- China, Russian Federation Supplier countries outside the EEA
- 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.