職責(zé)描述:1. Develop and execute RA strategy to get the approval and clearance from target countries for the medical de-vice. 發(fā)展和執(zhí)行醫(yī)療注冊(cè)事務(wù),...
職責(zé)描述: Establish and improve the regulatory documentations.創(chuàng)建并優(yōu)化注冊(cè)文檔Responsible for premarket products registration at CFDA, including d...