药品监管科学概论与质量源于设计
Introduction to Drug Regulatory Science with Quality by Design
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
药物安全:从非临床开发到药物警戒
Safety of Medicines: From Non-clinical Development to Pharmacovigilance
中国/美国/欧盟监管环境:程序和应用
China/USA/EU Regulatory Environment: Procedures and Applications
生物技术业务运营
Business Operations of Biotechnology
生物标志物和医疗器械
Biomarkers and Medical Devices
药物发现与开发
Drug Discovery and Development
营养保健品和转基因产品
Nutraceuticals and Transgenic Products
全球制药政策:理由和利益相关者
Global Pharmaceutical Policy: Rationales and Stakeholders
生物制药:质量开发和文档
Biopharmaceuticals: Quality Development and Documentation
药品安全中的大数据、人工智能和机器学习
Big Data, Artificial Intelligence and Machine Learning in Drug Safety
药品市场准入:趋势与挑战
Market Access for Pharmaceutical Products: Trends and Challenges
临床药理学和生物统计学
Clinical Pharmacology and Biostatistics
工业实习
Industrial Internship
监管事务顶点项目
Regulatory Affairs Capstone Project
产品开发管理
Product Development Management