EU active substance registration
Fidia Farmaceutici S.p.A.
EU active substance registration API/REG/37/2022/V · Italy
Key facts
| Registration number | API/REG/37/2022/V |
|---|---|
| EudraGMDP reference | 48996 |
| Registration holder | Fidia Farmaceutici S.p.A. |
| Registered site | Fidia Farmaceutici S.p.A. |
| Site address | Via Ponte Della Fabbrica 3 A, Abano Terme, 35031 |
| Country | Italy |
| Competent authority | IT_AIFA |
| National site reference | 27 |
| OMS location ID | LOC-100006290 |
| OMS organisation ID | ORG-100001641 |
| 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.