Работа regulatory affairs specialist в компании ANCOR в Москве

Main responsibilities: Perform full cycle of registration processes for medical devices as well as changes to the existing dossiers (VIRD, VIRU) Documents request from manufactures include working with manufacturers’ databases, share points or other ...

Main Responsibilities: Perform registration and certification/declaration processes for medical devices Documents request from manufactures include working with manufacturers’ databases, share points or other manufacturers’ sources Registration dossi...

Responsibilities: Planning and managing EAEU/RU national regulatory submissions of medicinal products and food supplement registration process according to the company business plan and in accordance with EAEU/RU regulatory requirements Involved in t...