EU active substance registration
Vemedia Manufacturing B.V.
EU active substance registration 17811 API · Netherlands
Key facts
| Registration number | 17811 API |
|---|---|
| EudraGMDP reference | 39931 |
| Registration holder | Vemedia Manufacturing B.V. |
| Registered site | Vemedia Manufacturing B.V. |
| Site address | Verrijn Stuartweg 60, Diemen, 1112 AX |
| Country | Netherlands |
| Competent authority | NL_FARMATEC |
| National site reference | FUSY/91269 |
| OMS location ID | LOC-100003132 |
| OMS organisation ID | ORG-100000418 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 1–9 Third-country API manufacturing sites
- China 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.