EU active substance registration
Tchaikapharma High Quality Medicines AD
EU active substance registration R-AV-V-020 · Bulgaria
Key facts
| Registration number | R-AV-V-020 |
|---|---|
| EudraGMDP reference | 47791 |
| Registration holder | Tchaikapharma High Quality Medicines AD |
| Registered site | Tchaikapharma High Quality Medicines AD |
| Site address | Blvd Sankt Peterburg 53, Plovdiv, 4000 |
| Country | Bulgaria |
| Competent authority | BG_BDA |
| National site reference | BG/GMP/2021/192 |
| OMS location ID | LOC-100000156 |
| OMS organisation ID | ORG-100000634 |
| EudraGMDP record | eudragmdp.ema.europa.eu |
At a glance
- 10–99 Third-country API manufacturing sites
- China, India, Mexico 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.