1985年11月1日起,卫生部根据《药品管理法》的有关规定,开始对全国新药实行统一审批。三年来,通过各方面的努力,在有关单位的支持下,中药新药的审批工作初步走上了规范化的轨道,新药审批工作的关系基本理顺。在技术方面,各级新药审评委员会专家的技术 From November 1, 1985, the Ministry of Health began to apply for unified approval of new drugs throughout the country in accordance with the relevant provisions of the Drug Administration Law. Over the past three years, through the efforts of various parties and with the support of the relevant units, the examination and approval of new drugs for traditional Chinese medicines has basically embarked on a standardized track, and the relationship between new drug approvals has been basically streamlined. In terms of technology, experts at all levels of the New Drug Review Committee