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序号 |
课程中文名称 |
课程英文名称 |
1 |
以质量源于设计的药品监管科学导论 |
Introduction to Drug Regulatory Science with Quality by Design |
2 |
药物、生物制剂和医疗器械开发:领导角色 |
Drugs, Biologics and Medical Devices Development: Leadership Role |
3 |
药物安全性:从非临床开发到药物警戒 |
Safety of Medicines: From Non-clinical Development to Pharmacovigilance |
4 |
中国/美国/欧盟监管环境:程序和应用 |
China/USA/EU Regulatory Environment: Procedures and Applications |
5 |
生物技术业务运营 |
Business Operations of Biotechnology |
6 |
生物标志物和医疗器械 |
Biomarkers and Medical Devices |
7 |
药物发现和开发 |
Drug Discovery and Development |
8 |
营养保健品和转基因产品 |
Nutraceuticals and Transgenic Products |
9 |
全球制药政策:基本原理和利益相关者 |
Global Pharmaceutical Policy: Rationales and Stakeholders |
10 |
生物制药:质量开发和文档 |
Biopharmaceuticals: Quality Development and Documentation |
11 |
大数据、人工智能和机器学习在药物安全中的应用 |
Big Data, Artificial Intelligence and Machine Learning in Drug Safety |
12 |
数字健康 |
Digital Health |
13 |
医药产品的市场准入:趋势与挑战 |
Market Access for Pharmaceutical Products: Trends and Challenges |
14 |
临床药理学和生物统计学 |
Clinical Pharmacology and Biostatistics |
15 |
行业实习 |
Industrial Internship |
16 |
法规事务顶点项目 |
Regulatory Affairs Capstone Project |
17 |
产品开发管理 |
Product Development Management |