Orion Corporation
Finnischer Pharma- und Diagnostikhersteller.
Orion Corporation ist ein finnisches Pharmaunternehmen, das proprietäre Arzneimittel, Generika und pharmazeutische Wirkstoffe (APIs) herstellt. Seine Tochtergesellschaft Fermion stellt APIs her, die an globale Pharmaunternehmen exportiert werden.
- Type
- brand seeking distribution
- Location
- Espoo, Finland
- Founded
- 1917
- Website
- orion.fi
- Categories
- Medizin- & Gesundheitsbedarf
- Markets
- Finnland, Deutschland, Schweden, Norwegen
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 Hier trägt der Zuschlag zusätzlich eine fremde Prüfung: In der EU und im EWR muss ein öffentlicher Auftraggeber Bieter ausschließen, die wegen Betrugs, Korruption oder Geldwäsche verurteilt sind, sowie solche, bei denen rechtskräftig festgestellte Steuer- oder Sozialabgabenschulden bestehen. 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)