PRO.MED.CS Praha a.s.
Manufaktur Farmasi, Czechia
PRO.MED.CS Praha a.s. adalah perusahaan manufaktur farmasi yang berbasis di Praha, Czechia. Terdaftar dalam daftar bisnis publik.
- Type
- Manufacturer
- Location
- Praha, Czechia
- Founded
- 1989
- Categories
- Manufaktur Farmasi
Listed in a source registry
Verified facts
- registered-manufacturer (green), checked 1989-02-01 ARES (Czech business register)
- public-contract-awarded (green), checked 2026-08-17 TED, EU public procurement bulletin Di sini kemenangan tender juga membawa pemeriksaan pihak lain: di UE dan EEA, pembeli publik wajib menggugurkan peserta yang dipidana karena penipuan, korupsi, atau pencucian uang, serta yang tunggakan pajak atau iurannya ditetapkan lewat putusan final. Directive 2014/24/EU, Article 57 (exclusion grounds)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-08-07 Finnish Medicines Agency (Fimea), basic register of medicinal products
- registry-active-global (green), checked 2026-08-24 ARES (Czech business register)
- registered-since (green), checked 1989-02-01 ARES (Czech business register)
- directors-on-file (green), checked 2026-08-24 ARES (Czech business register)
- leadership-on-record (green), checked 2024-06-26 ARES (Czech business register)
- gmp-certified (green), checked 2026-01-09 EudraGMDP, EU register of GMP certificates (EMA)
- export-registered (green), checked 2026-08-12 EU EORI validation (European Commission)
- 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)