KRKA, tovarna zdravil, d. d., Novo mesto
Sloveense industriële fabrikant en exporteur
KRKA, Tovarna Zdravil, ovl. d., Novo mesto wordt door Sloexport vermeld in de overige productiesector. Het directoryprofiel beschrijft activiteiten, waaronder Krka, behoort tot de top van generieke farmaceutische bedrijven ter wereld. De basisactiviteit van Krka bestaat uit de productie en verkoop van receptgeneesmiddelen, receptvrije producten en diergezondheidsproducten. De activiteiten van het bedrijf worden aangevuld met kuuroorden en toeristische diensten.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Novo Mesto, Slovenia
- Website
- https://krka.si
- Categories
- Farmaceutische productie, Medische en gezondheidszorgbenodigdheden
- Markets
- Slovenië, Oostenrijk, Duitsland, Italië, Kroatië
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)