
中国医疗行业法律法规中英数据库
第二章 医疗器械进口单位分类监管 Chapter II Classified Surveillance of Medical Instrument Importers第二章考试和注册 Chapter II Examination and Registration第二章考试和注册 Chapter II Examination and Registration第二章婚前保健 Chapter II Pre-marital Health Care第二章 预 防 CHAPTER II PREVENTION第二章设置审批 Chapter II The Examination & Approval Procedures for the Establishment of Medical Institutions第二章中药保护品种等级的划分和审批? CHAPTER II THE GRADING AND APPROVAL OF PROTECTION OF VARIETIES OF TRADITIONAL CHINESE MEDICINES第二章 精神药品的生产 Chapter II The Production of Psychotropic Drugs第三章药品经营企业的管理 CHAPTER III ADMINISTRATION OF DRUG-HANDLING ENTERPRISES 第三章 药品经营企业管理 Chapter III Administration of Pharmaceutical Trading Enterprises第三章孕产期保健 Chapter III Health Care During the Pregnant and Perinatal Period第三章执业登记 Chapter III Practice Registration第三章执业规则 Chapter III Practicing Rules第三章执业规则 Chapter III Practicing Rules第三章中药保护品种的保护? CHAPTER III PROTECTION OF THE PROTECTED VARIETIES OF TRADITIONAL CHINESE MEDICINES第三章 疫情的报告和公布 CHAPTER III REPORTING ON AND ANNOUNCING THE EPIDEMIC SITUATION第三章 进口医疗器械风险等级及检验监管 Chapter III Risk Levels and Inspection Supervision of Imported Medical Instruments第三章 精神药品的供应 Chapter III the Supply of Psychotropic Drugs第四章医疗单位的药剂管理 CHAPTER IV ADMINISTRATION OF DRUGS IN MEDICAL TREATMENT UNITS第四章 医疗机构的药剂管理 Chapter IV Administration of Pharmaceuticals at Medical Organizations第四章执业管理 Chapter IV Administration of Practice第四章 控 制 CHAPTER IV CONTROL第四章考核和培训 Chapter IV Evaluation and Training第四章考核和培训 Chapter IV Evaluation and Training第四章 进口捐赠医疗器械检验监管 Chapter IV Inspection Supervision on Imported Donated Medical Instruments语际翻译 版权所有
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