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Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary

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All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Based on a course taught by the editors at NIH, Ethical and Regulatory Aspects of Clinical Research is the first book designed to help investigators meet this new requirement. The book begins with the history of human subjects research a All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Based on a course taught by the editors at NIH, Ethical and Regulatory Aspects of Clinical Research is the first book designed to help investigators meet this new requirement. The book begins with the history of human subjects research and guidelines instituted since World War II. It then covers various stages and components of the clinical trial process: designing the trial, recruiting participants, ensuring informed consent, studying special populations, and conducting international research. Concluding chapters address conflicts of interest, scientific misconduct, and challenges to the IRB system. The appendix provides sample informed consent forms. This book will be used in undergraduate courses on research ethics and in schools of medicine and public health by students who are or will be carrying out clinical research. Professionals in need of such training and bioethicists also will be interested.


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All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Based on a course taught by the editors at NIH, Ethical and Regulatory Aspects of Clinical Research is the first book designed to help investigators meet this new requirement. The book begins with the history of human subjects research a All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Based on a course taught by the editors at NIH, Ethical and Regulatory Aspects of Clinical Research is the first book designed to help investigators meet this new requirement. The book begins with the history of human subjects research and guidelines instituted since World War II. It then covers various stages and components of the clinical trial process: designing the trial, recruiting participants, ensuring informed consent, studying special populations, and conducting international research. Concluding chapters address conflicts of interest, scientific misconduct, and challenges to the IRB system. The appendix provides sample informed consent forms. This book will be used in undergraduate courses on research ethics and in schools of medicine and public health by students who are or will be carrying out clinical research. Professionals in need of such training and bioethicists also will be interested.

37 review for Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary

  1. 5 out of 5

    loafingcactus

    The book consists entirely of primary sources from the history of medical research ethics. I can't imagine why anyone would use a different book for training in research ethics. The book consists entirely of primary sources from the history of medical research ethics. I can't imagine why anyone would use a different book for training in research ethics.

  2. 5 out of 5

    Amber Meriwether

  3. 5 out of 5

    Stephanie B.

  4. 5 out of 5

    Vanessa Merker

  5. 4 out of 5

    Dr. SamatraA "LS"

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    Angela

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    Kk Butler

  8. 5 out of 5

    Research4Researchers

  9. 5 out of 5

    Anne

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    Josh Lee

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  14. 5 out of 5

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  18. 5 out of 5

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  22. 4 out of 5

    Rachel Kirkland

  23. 5 out of 5

    Josh Lee

  24. 4 out of 5

    Cambray

  25. 4 out of 5

    Rodrigo Lopez

  26. 4 out of 5

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  27. 5 out of 5

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  30. 5 out of 5

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  31. 4 out of 5

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  33. 5 out of 5

    Marvin L Hooker Sr

  34. 4 out of 5

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  35. 5 out of 5

    Lara

  36. 4 out of 5

    John

  37. 5 out of 5

    Nicholassun

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