The Belmont Report PDF Download
Are you looking for read ebook online? Search for your book and save it on your Kindle device, PC, phones or tablets. Download The Belmont Report PDF full book. Access full book title The Belmont Report by United States. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. Download full books in PDF and EPUB format.
Author: United States. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research
Publisher:
ISBN:
Category : Ethics, Medical
Languages : en
Pages : 614
Get Book Here
Book Description
Author: United States. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research
Publisher:
ISBN:
Category : Ethics, Medical
Languages : en
Pages : 614
Get Book Here
Book Description
Author: United States. National Bioethics Advisory Commission
Publisher:
ISBN:
Category : Bioethics
Languages : en
Pages : 260
Get Book Here
Book Description
Author: United States. National Bioethics Advisory Commission
Publisher:
ISBN:
Category : Bioethics
Languages : en
Pages : 272
Get Book Here
Book Description
Author:
Publisher:
ISBN:
Category : Bioethics
Languages : en
Pages : 266
Get Book Here
Book Description
Author: United States. National Bioethics Advisory Commission
Publisher:
ISBN:
Category : Bioethics
Languages : en
Pages : 264
Get Book Here
Book Description
Author: United States. National Bioethics Advisory Commission
Publisher:
ISBN:
Category : Bioethics
Languages : en
Pages :
Get Book Here
Book Description
Author: Council for International Organizations of Medical Sciences (CIOMS)
Publisher: World Health Organization
ISBN: 9789290360889
Category : Bioethics
Languages : en
Pages : 0
Get Book Here
Book Description
"In the new 2016 version of the ethical guidelines, CIOMS provides answers to a number of pressing issues in research ethics. The Council does so by stressing the need for research having scientific and social value, by providing special guidelines for health-related research in low-resource settings, by detailing the provisions for involving vulnerable groups in research and for describing under what conditions biological samples and health-related data can be used for research."--Page 4 de la couverture.
Author: United States. National Bioethics Advisory Commission
Publisher:
ISBN:
Category : Bioethics
Languages : en
Pages :
Get Book Here
Book Description
Author: Elizabeth A. Bankert
Publisher: Jones & Bartlett Learning
ISBN: 9780763730499
Category : Medical
Languages : en
Pages : 568
Get Book Here
Book Description
This comprehensive reference covers three separate areas related to IRBs: administration, daily management; and ethical issues. This instructional manual provides IRB members and administrators with the information they need to run an efficient and effective system of protecting human research subjects, while remaining in compliance with federal research regulations. The text includes case studies, sample forms, and sample policy documents. The updated Second Edition includes seven new chapters: IRB Closure of Study Files, Internet Research, Research in Public Schools, Phase I Clinical Trials in Healthy Volunteers, Vulnerability in Research, Balancing the Risks and Potential Benefits,and HIPAA.
Author: Bartha Maria Knoppers
Publisher: BRILL
ISBN: 9047402936
Category : Law
Languages : en
Pages : 668
Get Book Here
Book Description
Genetic research and testing is not limited to individuals and their families. Increasingly, there is focus on communities and even whole populations. This raises legal and socio-ethical and issues that have not been addressed. In this age of international biobanking involving populations, are current legal and ethical approaches sufficient? This book of selected papers covers population research and banking as well as accompanying confidentiality, and governance concerns. Possible commercialization, patents, benefit sharing, discrimination, and the role of patient organizations and of developing countries are also discussed. New perspectives and models are provided. The book concludes with a Statement of Principles on the Ethical Conduct of Human Genetic Research Involving Populations. Policymakers, academics, legislators and researchers will find this book to be current and controversial. The human genome may be mapped but the legal and socio-ethical debate is far from over.
