從處方、制備工藝、質(zhì)量標準、特殊類藥材和外源性有害物質(zhì)的控制、包裝材料的相容性、現(xiàn)代分析技術(shù)及分析手段和數(shù)學(xué)方法的應(yīng)用及針對中藥注射劑的研究等幾方面對國家中藥評價性抽驗中的探索性研究工作進行探討，提出一些想法供同行參考。

In this paper, some considerations about exploratory study on evaluative tests of traditional Chinese medicine (TCM) were put forward, which were based on nine aspects as follows: prescription, preparation technology, quality standard, control of special medicinal materials and exogenous harmful substance, compatibility of packaging materials, application of modern analysis technology and mathematical method, and studies aiming at TCM injections. On the basis of these studies, some individual opinions were put forward for reference of pharmaceutical colleagues.