摘要
在精神医学临床研究中,精心设计并合理应用知情同意书能更好地发挥其对受试者的保护作用。本文对精神医学受试者知情同意书的设计进行简要介绍,阐述如何在研究中合理应用知情同意书,以期为我国精神医学临床研究中受试者知情同意书的设计与应用提供参考。
An informed consent form well-designed by researchers and pharmacists and its reasonable application are very important to protect the subjects in clinical psychiatric research. In this paper, the design of informed consent form was described,and how to use informed consent form reasonably was explained, in order to provide references for the design and application of informed consent form in clinical psychiatric research in China.
出处
《药学服务与研究》
CAS
CSCD
2012年第3期209-211,共3页
Pharmaceutical Care and Research
基金
国家科技重大专项重大新药创制资助项目(No.2012ZX09303-003)
关键词
知情同意书
伦理学
精神医学
临床研究
informed consent form
ethics
psychiatry
clinical research
