ICON
임상 연구, 제약, 의료 기기 채용 | ICON Plc 채용
ICON Plc에서 임상 연구, 제약, 생명공학 및 의료 기기 분야의 일자리를 찾아보세요. 임상 연구, 프로젝트 관리, 데이터 분석 등의 역할을 맡아 의료 발전을 전담하는 글로벌 팀과 협력하세요.
- Type
- distributor seeking brands
- Location
- Norway
- Website
- https://careers.iconplc.com
- Categories
- 의약품 제조, 의료 및 건강 관리 용품
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)