We're sorry this project doesn't work properly without JavaScript enabled. Please enable it to continue.
欢迎来到数字化实训平台
首页 - 课程列表 - 课程详情
美国药品医疗器械监管概述
课程类型:选修课
发布时间:2025-02-21 11:01:27
主讲教师:
课程来源:
建议学分:0.00分
课程编码:xtzx2156
1.FDA History, Structure, Function
2.New Drug Development Process/Pharmaceutical Industry Overview
3.Risk Management for Drugs and Devices
4.Patent Term Extension and Generic Exclusivity
5.Medical Device Development Process
6.Medical Device Industry Overview
7.FDA Postmarketing Surveillance Programs