Orion Corporation
Финский производитель фармацевтических и диагностических средств.
Orion Corporation , финская фармацевтическая компания, производящая патентованные лекарства, дженерики и активные фармацевтические ингредиенты (АФИ). Ее дочерняя компания Fermion производит АФИ, которые экспортируются мировым фармацевтическим компаниям.
- Type
- brand seeking distribution
- Location
- Espoo, Finland
- Founded
- 1917
- Website
- orion.fi
- Categories
- Медицинские товары и расходники
- Markets
- Финляндия, Германия, Швеция, Норвегия
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 Здесь награда несёт ещё и чужую проверку: в ЕС и ЕЭЗ заказчик обязан отстранить участника, осуждённого за мошенничество, коррупцию или отмывание, и того, за кем окончательным решением признаны долги по налогам или социальным взносам. 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)