创新制剂及其营销创新的法律基础--美国案例分析

来源 :2015年中国药物制剂大会、中国药学会药剂专业委员会2015年学术年会暨国际控释协会中国分会2015年学术年会 | 被引量 : 0次 | 上传用户:lsh19
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  The most important aspect of a generic drug approval is perhaps the therapeutic equivalence (TE) between the generic drug and the referenced brand drug, as TE will often lead to mandatory prescription substitution thus saving a generic drug maker's cost of doing marketing work.
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