“新药审批办法”药理毒理工作研讨会于1987年9月11～16日在青岛召开。会议代表来自25个省市自治区共298人。会期5天。两年来,药学工作者在执行“新药审批办法”过程中,遇到了许多实际问题,也积累了许多经验。通过这次会议,代表们交流了学术观点,为“新药审批办法”药理毒理工作提出了补充修改意见和建议。此外,解决了一些在新药开发和新药审批过程中的具体问题,如对新药研制中的药效学、药代动力学、毒理学的试验,进 “New drug approval approach ” Pharmacology and Toxicology Seminar held in Qingdao on September 11 ~ September 1987. The delegates from a total of 298 people from 25 provinces. Duration of 5 days. In the past two years, pharmacy practitioners have encountered many practical problems and accumulated a great deal of experience in the implementation of the “Measures for the Approval of New Drugs.” Through this meeting, the deputies exchanged views on academic issues and proposed additional amendments and suggestions for the “new drug approval measures” pharmacological and toxicological work. In addition, some specific problems in the process of drug development and approval of new drugs have been solved, such as pharmacodynamics, pharmacokinetics and toxicology tests in the development of new drugs,