ICON
临床研究、制药、医疗器械工作 | ICON Plc 职业机会
探索 ICON Plc 的临床研究、制药、生物技术和医疗设备方面的职位。与致力于推进医疗保健的全球团队合作，在临床研究、项目管理、数据分析等方面发挥作用。
- Type
- distributor seeking brands
- Location
- Norway
- Website
- https://careers.iconplc.com
- Categories
- 药品制造, 医疗保健用品
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)