Institutional Review Board: Member Handbook
暫譯: 機構審查委員會:成員手冊
Amdur, Robert J., Bankert, Elizabeth A.
- 出版商: Jones & Bartlett Publishers
- 出版日期: 2021-01-29
- 售價: $4,130
- 貴賓價: 9.8 折 $4,047
- 語言: 英文
- 頁數: 220
- 裝訂: Quality Paper - also called trade paper
- ISBN: 128419714X
- ISBN-13: 9781284197143
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相關分類:
專案管理 PM
海外代購書籍(需單獨結帳)
相關主題
商品描述
From new technology to the management of big data, and globalization of research, navigating the processes for preparing and conducting research studies involving human subjects is challenging and complicated. Designed to give Institutional Review Board (IRB) members the information they need to protect the rights and welfare of research subjects in a way that is both effective and efficient, the chapters of the Institutional Review Board: Member Handbook are short and to the point. Topic-specific chapters list the criteria IRB members should use to determine how to vote on specific kinds of studies and offer practical advice on what IRB members should do before and during full-committee meetings. The Fourth Edition includes the new federal guidelines for IRBs that went into effect in January 2019 and is an excellent accompaniment to Institutional Review Board: Management and Function, Third Edition (ISBN: 978-1-284-18115-9). The book has three sections: -Part 1: Preliminary Information contains background information on human subject research and a brief history of the IRB system -Part 2: The Full Committee IRB Meeting focuses on the research proposal review process -Part 3: Specific Topics covers advertising for research, conflict of interest, qualitative methods, informed consent, research involving children and prisoners, and deception of research subjects
商品描述(中文翻譯)
從新技術到大數據管理,以及研究的全球化,準備和進行涉及人類受試者的研究研究過程既具挑戰性又複雜。為了讓機構審查委員會(IRB)成員獲得保護研究受試者權利和福祉所需的信息,並以有效且高效的方式進行,機構審查委員會:成員手冊的各章節簡短且切中要點。針對特定主題的章節列出了IRB成員應使用的標準,以決定如何對特定類型的研究進行投票,並提供了有關IRB成員在全委會會議前和會議期間應該做什麼的實用建議。第四版包括自2019年1月生效的新聯邦IRB指導方針,是《機構審查委員會:管理與功能》第三版(ISBN: 978-1-284-18115-9)的極佳補充。該書分為三個部分:
- 第1部分:初步信息包含有關人類受試者研究的背景信息和IRB系統的簡要歷史
- 第2部分:全委會IRB會議專注於研究提案審查過程
- 第3部分:特定主題涵蓋研究廣告、利益衝突、定性方法、知情同意、涉及兒童和囚犯的研究,以及對研究受試者的欺騙