Medical Science is a delicate subject and the clinical data generated from the medical trials must be reliable and of good quality. Not only the quality of generated data is important, but the management is also crucial and is to be handled very carefully. In this paper, the ethical aspect ...
Ethics: Today's Hot Topics Arthur L. Caplan, PhD CDC Expert Commentary Mandrola on Medscape John M. Mandrola, MD Impact Factor with F. Perry Wilson F. Perry Wilson, MD, MSCE Medscape Essentials Medscape App Access what you need, when you need it. Download the app. New! 2024 ...
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The American Medical Association's (AMA's) 1957 Principles of Medical Ethics enjoins doctors to report accidents, injuries, or poor results stemming from medical treatment [67]. The AMA's 2001 revised Principles states that physicians must be honest with patients and expose incompetent or unethical...
- 《Bmc Medical Ethics》 被引量: 64发表: 2007年 Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from South Africa BMC Medical Ethics, 8, 5.Slack C, Strode A, Fleischer T, et al. Enrolling adolescents in HIV vaccine trials: reflections on legal complexities from...
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In clinical trials, the protocol must also describe appropriate arrangements for post-trial provisions. Research Ethics Committees 23. The research protocol must be submitted for consideration, comment, guidance and approval to the concerned research ethics committee before the study begins. This committe...
Ethics & law in medical discovery,clinical trials,& digital health records 来自 万方 喜欢 0 阅读量: 22 作者: DJ Palmisano 摘要: The 21st Century brings the promise of great medical discoveries as we unravel the mysteries of the human ge nome with the promise of new therapies developed for ...
In this case, we recommend a practical clinical application or a test with a different dataset than the one used to design the algorithm or model – an evaluation performed with data from other facilities is recommended. In other words, the dataset must be different (origin and testing). In...
Informed consent in clinical trials in critical care: experience from the PAC-Man Study OBJECTIVES: To identify the proportion of critically ill patients able to consent to participation in a randomised controlled trial (RCT) and to assess to ......