药学,药品注册,药品销售人员必备知识!
814 医疗器械的上市前批准 PREMARKET APPROVAL OF MEDICAL DEVICES
820 质量体系规章 QUALITY SYSTEM REGULATION
821 医疗器械跟踪要求 MEDICAL DEVICE TRACKING REQUIREMENTS
822 上市后监视 POSTMARKET SURVEILLANCE
860 医疗器械分类程序 MEDICAL DEVICE CLASSIFICATION PROCEDURES
861 性能标准制定程序 PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
862 临床化学与临床毒理学器械 CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
864 血液学与病理学器械 HEMATOLOGY AND PATHOLOGY DEVICES
866 免疫学与微生物学器械 IMMUNOLOGY AND MICROBIOLOGY DEVICES
868 麻醉学器械 ANESTHESIOLOGY DEVICES
870 心血管器械 CARDIOVASCULAR DEVICES
872 牙科器械 DENTAL DEVICES
874 耳、鼻和咽器械 EAR, NOSE, AND THROAT DEVICES
876 胃肠病学-泌尿学器械 GASTROENTEROLOGY-UROLOGY DEVICES
878 普通与整形外科器械 GENERAL AND PLASTIC SURGERY DEVICES
880 普通医院与个人使用器械 GENERAL HOSPITAL AND PERSONAL USE DEVICES
882 神经学器械 NEUROLOGICAL DEVICES
884 产科与妇科学器械 OBSTETRICAL AND GYNECOLOGICAL DEVICES
886 眼科器械 OPHTHALMIC DEVICES
888 矫形外科器械 ORTHOPEDIC DEVICES
890 内科学器械 PHYSICAL MEDICINE DEVICES
892 放射学器械 RADIOLOGY DEVICES
895 禁止的器械 BANNED DEVICES
898 电极铅线与患者电缆的性能标准 PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES 第I分章―乳房造影质量标准法（SUBCHAPTER I―MAMMOGRAPHY QUALITY STANDARDS ACT）
900 乳房造影法 MAMMOGRAPHY
第J分章―放射学的健康（SUBCHAPTER J―RADIOLOGICAL HEALTH）
1000 总则 GENERAL
1002 记录与报告 RECORDS AND REPORTS
1003 缺陷与未能守法的通报 NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
1004 电子产品的回购、修理或者置换 REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS
1005 电子产品的进口 IMPORTATION OF ELECTRONIC PRODUCTS
1010 电子产品的性能标准：总则 PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL
1020 电离辐射发生产品的性能标准 PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
1030 微波与射电频率发生产品的性能标准 PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS
1040 发光产品的性能标准 PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
1050 声波、次声波和超声波发生产品的性能标准 PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS
第K分章―[预留的]（SUBCHAPTER K―[RESERVED]）
第L分章―根据由食品与药品管理局行政执行的某些其他法的规章（SUBCHAPTER L―REGULATIONS UNDER CERTAIN OTHER ACTS ADMINISTERED BY THE FOOD AND DRUG ADMINISTRATION）
1210 根据《联邦进口乳法》的规章 REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT
1230 根据《联邦腐蚀性毒物法》的规章 REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
1240 传染病的控制 CONTROL OF COMMUNICABLE DISEASES
1250 州际运输卫生 INTERSTATE CONVEYANCE SANITATION
1251-1269 [预留的] [Reserved]
1270 预期用于移植的人体组织 HUMAN TISSUE INTENDED FOR TRANSPLANTATION
1271 人体细胞、组织以及细胞的和基于组织的产品 HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS 1272-1299 [预留的] [Reserved]
第Ⅱ章―司法部毒品强制执行局（CHAPTER Ⅱ―DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE） 1300 定义 DEFINITIONS
1301 管制物质的制造者、分销者和调剂者的登记 REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, AND DISPENSERS OF CONTROLLED SUBSTANCES
1302 对管制物质的标识与包装要求 LABELING AND PACKAGING REQUIREMENTS FOR CONTROLLED SUBSTANCES 1303 定额 QUOTAS
1304 登记者的记录与报告 RECORDS AND REPORTS OF REGISTRANTS
1305 令的格式 ORDER FORMS
1306 处方 PRESCRIPTIONS
1307 杂项 MISCELLANEOUS
1308 管制物质的表 SCHEDULES OF CONTROLLED SUBSTANCES
1309 表I化学品的制造者、分销者、进口者和出口者的登记 REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, IMPORTERS AND EXPORTERS OF LIST I CHEMICALS
1310 列入表的化学品和某些机器的记录与报告 RECORDS AND REPORTS OF LISTED CHEMICALS AND CERTAIN MACHINES 1311 [预留的] [Reserved]
1312 管制物质的进口与出口 IMPORTATION AND EXPORTATION OF CONTROLLED SUBSTANCES
1313 前体与必要化学品的进口与出口 IMPORTATION AND EXPORTATION OF PRECURSORS AND ESSENTIAL CHEMICALS