ICON
Pekerjaan Penelitian Klinis, Farmasi, Alat Kesehatan | Karir ICON Plc
Jelajahi pekerjaan di bidang Penelitian Klinis, Farmasi, Bioteknologi & Alat Kesehatan di ICON Plc. Bekerja dengan tim global yang berdedikasi untuk memajukan layanan kesehatan dengan peran dalam penelitian klinis, manajemen proyek, analisis data, dan banyak lagi.
- Type
- distributor seeking brands
- Location
- Norway
- Website
- https://careers.iconplc.com
- Categories
- Manufaktur Farmasi, Perlengkapan Medis & Kesehatan
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)