EU active substance registration
Pharma Greven GmbH
EU active substance registration DE_NW_05_Reg_2019_0001/24.05.03-011 · Germany
Key facts
| Registration number | DE_NW_05_Reg_2019_0001/24.05.03-011 |
|---|---|
| EudraGMDP reference | 14108 |
| Registration holder | Pharma Greven GmbH |
| Registered site | Pharma Greven GmbH |
| Site address | Hüttruper Heide 90, Greven, 48268 |
| Country | Germany |
| Competent authority | DE_NW_05 |
| National site reference | 24.05.03-011 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- None Third-country API manufacturing sites
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.