| 缩写 | 全称 | 中文释义 |
|---|---|---|
| PS (CDER) | Planning Staff (OC) | 规划人员(OC) |
| OC (CFSAN) | Office of Compliance (CFSAN) | 合规办公室(CFSAN) |
| CTM | Clinical Trials Material | 临床试验材料 |
| EREA | Export Reform and Enhancement Act of 1996 | 1996年《出口改革和加强法》 |
| EEPS | Electronic Entry Processing System | 电子出入境处理系统 |
| ICH | International Conference on Harmonization (of Technical Requirements for Registration of Pharmaceuticals for Human Use) | 国际协调会议(人用药品注册技术要求) |
| AIRIO | Agency Intramural Research Integrity Officer | 机构内部研究诚信官 |
| DTD | Division of Training and Development | 培训与发展司 |
| PMHS (CDER) | Pediatric and Maternal Health Staff (CDER) | 儿科和产妇保健人员(CDER) |
| CPMP | Committee for Proprietary Medicinal Products | 专卖医药产品委员会 |