20 Октября
Senior Regulatory Affairs Specialist
Москва
Компания "ANCOR" 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 manufacturers’ sources Registration dossier preparation (development of local technical files, IFU and other related...
19 Октября
Москва
Компания "ANCOR" 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 the process of creating the strategies for registration and maintenance of MP in EAEU/RU Preparation of dossiers,...