EU active substance registration
UNI-PHARMA ΚΛΕΩΝ ΤΣΕΤΗΣ ΦΑΡΜΑΚΕΥΤΙΚΑ ΕΡΓΑΣΤΗΡΙΑ ΑΒΕΕ / UNI-PHARMA KLEON TSETIS PHARMACEUTICAL LABORATORIES SA
EU active substance registration 00000020/20/1 · Greece
Key facts
| Registration number | 00000020/20/1 |
|---|---|
| EudraGMDP reference | 1734 |
| Registration holder | UNI-PHARMA ΚΛΕΩΝ ΤΣΕΤΗΣ ΦΑΡΜΑΚΕΥΤΙΚΑ ΕΡΓΑΣΤΗΡΙΑ ΑΒΕΕ / UNI-PHARMA KLEON TSETIS PHARMACEUTICAL LABORATORIES SA |
| Registered site | UNI-PHARMA ΚΛΕΩΝ ΤΣΕΤΗΣ ΦΑΡΜΑΚΕΥΤΙΚΑ ΕΡΓΑΣΤΗΡΙΑ ΑΒΕΕ / UNI-PHARMA KLEON TSETIS PHARMACEUTICAL LABORATORIES SA |
| Site address | 14ο χλμ Εθνικής Οδού 1 / 14th km National Road 1, Κτήριο Α / Building A & Κτήριο Β / Building B, Κάτω Κηφισιά Αττικής / Kato Kifisia Attiki, 14564 |
| Country | Greece |
| Competent authority | GR_NOM |
| National site reference | 0000000020 |
| OMS location ID | LOC-100000167 |
| OMS organisation ID | ORG-100000348 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 1–9 Third-country API manufacturing sites
- Switzerland 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.