Abstract: The bioequivalent test in human belongs to clinical trial range.The medical institutions should strictly carry out the state laws and obey rules and regulations,the good clinical practice, and the interrelated clinical trial international laws.In technology, all clinical activity should try its best to the demand of standard operation procedure and to accord with the different principle of technique guidance and the standards.The items of charge and accounting management should be specification and reasonable.The prices gradually tend to its perfecting system.

Key words: clinical trials phase I, bioequivalenct trial, item charge, cost accounting, price management