ICON
臨床研究、製薬、医療機器の求人 | ICON Plc の採用情報
ICON Plc で臨床研究、製薬、バイオテクノロジー、医療機器の求人を探してみましょう。臨床研究、プロジェクト管理、データ分析などの役割を担い、医療の進歩に専念するグローバル チームと協力してください。
- Type
- distributor seeking brands
- Location
- Norway
- Website
- https://careers.iconplc.com
- Categories
- 医薬品製造, 医療およびヘルスケア用品
Verified facts
- registry-active-global (green), checked 2026-07-09 Brønnøysund (Enhetsregisteret)
- lei-lapsed (amber), checked 2026-07-09 GLEIF
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)
- 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)