EU active substance registration
Biotika, a.s.
EU active substance registration SK/002A/2018 · SLOVAKIA
Key facts
| Registration number | SK/002A/2018 |
|---|---|
| EudraGMDP reference | 4305 |
| Registration holder | BIOTIKA a.s. |
| Registered site | Biotika, a.s. |
| Site address | Slovenská Ľupča č. 566, Slovenská Ľupča, 976 13 |
| Country | SLOVAKIA |
| Competent authority | SK_SIDC |
| National site reference | V006 |
| OMS location ID | LOC-100003428 |
| OMS organisation ID | ORG-100001428 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 1–9 Third-country API manufacturing sites
- India Supplier countries outside the EEA
- 10–99 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.