国家药物政策与药监管+药学、药师、药学职业道德.pptVIP

第二章  国家药物政策 药品监管 National Medicine Policy  Drug Administration 第一节 药 品 一、药品的定义 《中华人民共和国药品管理法》中关于药品的定义是：“药品：指用于预防、治疗、诊断人的疾病，有目的地调节人的生理机能并规定有适应证或者功能与主治、用法和用量的物质，包括中药材、中药饮片、中成药、化学原料药及其制剂、抗生·素、生化药品、放射性药品、血清、疫苗、血液制品和诊断药品等。” Definition of drugs in “The Drug Administration Law of P.R.C” Drugs: refer to those substances used for the prevention, treatment and diagnosis of human diseases, and for the intentional regulation of human physiological functions. For which indications or actions, usage and dosage have been established. Including herbal drugs and their preparations,