药物制剂是防病治病的物质基础.在国外几乎全部由药厂来承担,在我国至今相当部分的临床药物制剂仍由医院制剂室来制备。自1985年7月1日在全国执行《药品管理法》之后,各地有关部门都加强了药品质量的全面管理,有效地促进了药品质量的提高。近五年来我地区各医疗单位(包括县级医院)自制制剂的抽验合格率,每年平均递增6.36％,1985年底达81.9％.南宁市各医院自制制剂抽验合格率1986年也仅达78.2％,说明了在我区医院自制制剂的质量上还存在着不少问题。为了促使其质量进一步全面的提高,应对影响质量的各因素进行分析研究,下面分两部分来叙述: 一、医院自制的输液制剂从配制的数量和技术要求来看,它均是医院制剂的主要 Drug preparations are the material basis for disease prevention and treatment. Almost all foreign companies are borne by pharmaceutical companies. In China, a considerable part of clinical drug preparations are still prepared by hospital preparation rooms. Since the “Drug Administration Law” was implemented nationwide on July 1, 1985, all local authorities have strengthened the overall management of drug quality and effectively promoted the improvement of drug quality. In the past five years, the qualified rate of self-made testing of medical units (including county-level hospitals) in our region has increased by an average of 6.36% per year and reached 81.9% by the end of 1985. The passing rate of self-made testing in Nanning hospitals has only reached 78.2% in 1986. It shows that there are still many problems in the quality of self-made preparations in our hospital. In order to promote further and comprehensive improvement of its quality, various factors affecting quality are analyzed and researched. The following are two parts to describe: First, the hospital’s self-made infusion preparations are mainly based on the quantity and technical requirements of formulation.