KRKA, tovarna zdravil, d. d., Novo mesto
Sloven endüstriyel üretici ve ihracatçı
KRKA, tovarna zdravil, d. d., Novo mesto Sloexport tarafından diğer imalat sektöründe listelenmiştir. Dizin profili, Krka'nın dünyadaki en iyi jenerik ilaç şirketleri arasında yer alması da dahil olmak üzere operasyonlarını açıklamaktadır. Krka'nın temel faaliyet alanı reçeteli ilaçlar, reçetesiz ürünler ve hayvan sağlığı ürünlerinin üretimi ve satışıdır. Şirketin faaliyetleri sağlık tesisi ve turistik hizmetler ile desteklenmektedir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Novo Mesto, Slovenia
- Website
- https://krka.si
- Categories
- İlaç Üretimi, Tıbbi ve Sağlık Malzemeleri
- Markets
- Slovenya, Avusturya, Almanya, İtalya, Hırvatistan
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- lei-active (green), checked 2026-08-09 GLEIF
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- domain-registered (green), checked 2026-08-09 Domain registry record
- gmp-certified (green), effective since 2026-04-02 EudraGMDP, EU register of GMP certificates (EMA)
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)