EU active substance registration
BIEFFE MEDITAL S.P.A.
EU active substance registration AMA - 16/2017 · Italy
Key facts
| Registration number | AMA - 16/2017 |
|---|---|
| EudraGMDP reference | 9685 |
| Registered site | BIEFFE MEDITAL S.P.A. |
| Country | Italy |
| Competent authority | IT_AIFA |
| National site reference | 100192 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 1–9 Third-country API manufacturing sites
- United States Supplier countries outside the EEA
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.