临床试验
知情同意
临床研究
工程伦理学
医学
伦理问题
研究伦理
替代医学
病理
工程类
作者
Ana Cristina Ramalhinho,Miguel Castelo‐Branco
标识
DOI:10.1007/978-1-0716-0872-2_17
摘要
Several experimental human DNA vaccines are currently undergoing Phase I, II, and III clinical trials in order to investigate their efficacy and safety. Human clinical trials must follow guidelines and procedures that have been approved by the regulatory authorities and ethics committees. Ethical clinical research is much more than applying an informed consent to participants. In this chapter we will review the ethical standards and provide a framework to evaluate and design ethical clinical research. Despite being universal standards supported by universal guidelines, they must be adapted to the conditions in each country where the clinical research is being conducted.
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