EU active substance registration
Farmaceutisch Analytisch Laboratorium Duiven B.V.
EU active substance registration 6264 API · Netherlands
Key facts
| Registration number | 6264 API |
|---|---|
| EudraGMDP reference | 1597 |
| Registration holder | Farmaceutisch Analytisch Laboratorium Duiven B.V. |
| Registered site | Farmaceutisch Analytisch Laboratorium Duiven B.V. |
| Site address | Dijkgraaf 30, Duiven, 6921 RL |
| Country | Netherlands |
| Competent authority | NL_FARMATEC |
| National site reference | 1711623367363 |
| OMS location ID | LOC-100031228 |
| OMS organisation ID | ORG-100022548 |
| 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.