Bio-Optronics Inc. Rochester NY.
Semin Oncol Nurs. 2020 Apr;36(2):151001. doi: 10.1016/j.soncn.2020.151001. Epub 2020 Apr 4.
To explore the federal regulations governing clinical trials and human subject protection, the importance of research participant's informed consent, and the role the oncology clinical research nurse has within the clinical trial setting.
Peer-reviewed journal articles, internet, book chapters, white papers.
Federal regulations mandate the conduct of a clinical research trial, human research participant protection, and the informed consent process.
The oncology nurse supports the autonomy and safe conduct of the human research participant during a clinical research trial and provides education and support through the informed consent process.
探讨联邦法规对临床试验和人体受试者保护的规定、研究参与者知情同意的重要性，以及肿瘤临床研究护士在临床试验环境中的作用。
同行评议的期刊文章、互联网、书籍章节、白皮书。
联邦法规规定了临床研究试验的进行、人体研究参与者的保护以及知情同意过程。
肿瘤护士在临床研究试验期间支持人体研究参与者的自主权和安全，并通过知情同意过程提供教育和支持。
