ARDEAPHARMA, a.s.
捷克药品制造
ARDEPHARMA 有限公司是一家总部位于捷克Ševětín 的制药公司。在公共企业登记处列出。
- Type
- Manufacturer
- Location
- Ševětín, Czechia
- Founded
- 2019
- Categories
- 药品制造
Listed in a source registry
Verified facts
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- registry-active-global (green), checked 2026-08-24 ARES (Czech business register)
- registered-since (green), checked 2019-03-06 ARES (Czech business register)
- directors-on-file (green), checked 2026-08-24 ARES (Czech business register)
- leadership-on-record (green), checked 2023-03-31 ARES (Czech business register)
- gmp-certified (green), checked 2026-05-14 EudraGMDP, EU register of GMP certificates (EMA)
- export-registered (green), checked 2026-08-12 EU EORI validation (European Commission)
- registered-manufacturer (green), checked 2019-03-06 ARES (Czech business register)
- vat-valid (green), checked 2026-08-08 VIES (European Commission)
- registry-id-verified (green), checked 2026-07-04 ARES (Ministry of Finance) + Verejny rejstrik a Sbirka listin (Ministry of Justice)
- workforce-on-record (green), checked 2026-08-16 ARES, registr ekonomických subjektů (Česká republika)
Claimed certifications
- Good Manufacturing Practice
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)