Orion Corporation
Fabricant finlandais de produits pharmaceutiques et de diagnostics.
Orion Corporation est une société pharmaceutique finlandaise produisant des médicaments exclusifs, des médicaments génériques et des ingrédients pharmaceutiques actifs (API). Sa filiale Fermion fabrique des API exportés vers des sociétés pharmaceutiques mondiales.
- Type
- brand seeking distribution
- Location
- Espoo, Finland
- Founded
- 1917
- Website
- orion.fi
- Categories
- Fournitures médicales et de santé
- Markets
- Finlande, Allemagne, Suède, Norvège
Verified facts
- gmp-certified (green), checked 2024-12-12 EudraGMDP, EU register of GMP certificates (EMA)
- domain-registered (green), checked 2026-08-02 Domain registry record
- supervised-operator (green), checked 2026-08-14 Tukes register of operators (Finnish Safety and Chemicals Agency)
- places-goods-on-market (green), checked 2026-08-07 Finnish Medicines Agency (Fimea), basic register of medicinal products
- public-contract-awarded (green), checked 2025-04-23 TED (Tenders Electronic Daily), EU public procurement award notices Ici l'attribution porte aussi un contrôle fait par d'autres: dans l'UE et l'EEE, l'acheteur public doit exclure les candidats condamnés pour fraude, corruption ou blanchiment, ainsi que ceux dont une décision définitive a établi des dettes fiscales ou sociales. Directive 2014/24/EU, Article 57 (exclusion grounds)
- registered-address (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registry-active-global (green), checked 2026-07-09 Finnish Patent and Registration Office (PRH)
- tax-filing-active (green), checked 2026-08-14 Finnish Tax Administration, public corporate tax data 2024 (Verohallinto)
- registry-id-verified (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registry-activity (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)