Stages Of Development Of Generic Drugs   Oral Solid Preparations, Tablets   1. Chemical Properties, Production And Control In The Development Of Oral Solid Preparations   Through the analysis of the components within the packaging material of the control drug, the basic information about the control drug is obtained   (1) Prescription ingredients   (2) […]

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This paper summarizes and draws up the decision tree for the in vitro consistency evaluation of oral solid generic drugs in combination with the relevant technical requirements such as “Requirements for Application Materials for Consistency Evaluation of the Quality and Efficacy of Oral Solid Preparations of Chemical Generic Drugs (Trial)”, and discusses the in vitro