EU active substance registration
Rodisma-Med Pharma GmbH
EU active substance registration DE_NW_04_Reg_2019_0003 · Germany
Key facts
| Registration number | DE_NW_04_Reg_2019_0003 |
|---|---|
| EudraGMDP reference | 14011 |
| Registration holder | Rodisma-Med Pharma GmbH |
| Registered site | Rodisma-Med Pharma GmbH |
| Site address | Koelner Strasse 48, Koeln, Nordrhein-Westfalen, 51149 |
| Country | Germany |
| Competent authority | DE_NW_04 |
| National site reference | 00017188 |
| OMS location ID | LOC-100010701 |
| OMS organisation ID | ORG-100007886 |
| 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.