Ethical and Policy Issues in International Research - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Ethical and Policy Issues in International Research write by United States. National Bioethics Advisory Commission. This book was released on 2001. Ethical and Policy Issues in International Research available in PDF, EPUB and Kindle.
International Ethical Guidelines for Health-Related Research Involving Humans
International Ethical Guidelines for Health-Related Research Involving Humans - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook International Ethical Guidelines for Health-Related Research Involving Humans write by Council for International Organizations of Medical Sciences (CIOMS). This book was released on 2017-01-31. International Ethical Guidelines for Health-Related Research Involving Humans available in PDF, EPUB and Kindle. "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.
Sharing Clinical Trial Data
Sharing Clinical Trial Data - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Sharing Clinical Trial Data write by Institute of Medicine. This book was released on 2015-04-20. Sharing Clinical Trial Data available in PDF, EPUB and Kindle. Data sharing can accelerate new discoveries by avoiding duplicative trials, stimulating new ideas for research, and enabling the maximal scientific knowledge and benefits to be gained from the efforts of clinical trial participants and investigators. At the same time, sharing clinical trial data presents risks, burdens, and challenges. These include the need to protect the privacy and honor the consent of clinical trial participants; safeguard the legitimate economic interests of sponsors; and guard against invalid secondary analyses, which could undermine trust in clinical trials or otherwise harm public health. Sharing Clinical Trial Data presents activities and strategies for the responsible sharing of clinical trial data. With the goal of increasing scientific knowledge to lead to better therapies for patients, this book identifies guiding principles and makes recommendations to maximize the benefits and minimize risks. This report offers guidance on the types of clinical trial data available at different points in the process, the points in the process at which each type of data should be shared, methods for sharing data, what groups should have access to data, and future knowledge and infrastructure needs. Responsible sharing of clinical trial data will allow other investigators to replicate published findings and carry out additional analyses, strengthen the evidence base for regulatory and clinical decisions, and increase the scientific knowledge gained from investments by the funders of clinical trials. The recommendations of Sharing Clinical Trial Data will be useful both now and well into the future as improved sharing of data leads to a stronger evidence base for treatment. This book will be of interest to stakeholders across the spectrum of research-from funders, to researchers, to journals, to physicians, and ultimately, to patients.
Ethical and Policy Issues in International Research
Ethical and Policy Issues in International Research - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Ethical and Policy Issues in International Research write by United States. National Bioethics Advisory Commission. This book was released on 2001. Ethical and Policy Issues in International Research available in PDF, EPUB and Kindle.
Ethical Conduct of Clinical Research Involving Children
Ethical Conduct of Clinical Research Involving Children - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Ethical Conduct of Clinical Research Involving Children write by Institute of Medicine. This book was released on 2004-07-09. Ethical Conduct of Clinical Research Involving Children available in PDF, EPUB and Kindle. In recent decades, advances in biomedical research have helped save or lengthen the lives of children around the world. With improved therapies, child and adolescent mortality rates have decreased significantly in the last half century. Despite these advances, pediatricians and others argue that children have not shared equally with adults in biomedical advances. Even though we want children to benefit from the dramatic and accelerating rate of progress in medical care that has been fueled by scientific research, we do not want to place children at risk of being harmed by participating in clinical studies. Ethical Conduct of Clinical Research Involving Children considers the necessities and challenges of this type of research and reviews the ethical and legal standards for conducting it. It also considers problems with the interpretation and application of these standards and conduct, concluding that while children should not be excluded from potentially beneficial clinical studies, some research that is ethically permissible for adults is not acceptable for children, who usually do not have the legal capacity or maturity to make informed decisions about research participation. The book looks at the need for appropriate pediatric expertise at all stages of the design, review, and conduct of a research project to effectively implement policies to protect children. It argues persuasively that a robust system for protecting human research participants in general is a necessary foundation for protecting child research participants in particular.
