Outreach Notebook for the NIH Guidelines on Inclusion of Women and Minorities as Subjects in Clinical Research PDF Download
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Author: National Institutes of Health (U.S.)
Publisher:
ISBN:
Category : Human experimentation in medicine
Languages : en
Pages : 37
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Book Description
Author: National Institutes of Health (U.S.)
Publisher:
ISBN:
Category : Human experimentation in medicine
Languages : en
Pages : 37
Get Book Here
Book Description
Author: National Institutes of Health (U.S.)
Publisher:
ISBN:
Category : Human experimentation in medicine
Languages : en
Pages : 164
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Book Description
Author: National Institutes of Health (U.S.)
Publisher:
ISBN:
Category : Human experimentation in medicine
Languages : en
Pages : 96
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Book Description
Author: National Institutes of Health (U.S.)
Publisher:
ISBN:
Category : Human experimentation in medicine
Languages : en
Pages :
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Book Description
Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Book Description
Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 188
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Book Description
Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 188
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Book Description
Author: Evan DeRenzo
Publisher: Elsevier
ISBN: 0080454208
Category : Medical
Languages : en
Pages : 321
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Book Description
This highly engaging guide for clinical researchers provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. Writing Clinical Research Protocols includes practical information on ethical principles in clinical research, designing appropriate research studies, writing consent and assent documents, getting protocols approved, special populations, confidentiality issues, and the reporting of adverse events. A valuable appendix includes a listing of web resources about research ethics as well as a glossary. This is an invaluable resource for basic scientists collaborating in clinical trials, physician investigators, clinical research fellows, research nurse coordinators, residents, and anyone who wants a better understanding of the clinical trials process. - Walks investigators and trainees through identification of the ethical aspects of each section of a clinical research protocol - Includes a chapter containing Case Histories - Contains information on conducting clinical research within the pharmaceutical industry - An appendix includes internet resources and world wide web addresses for important research ethics documents and regulations - Chapter on 'Study Design and Methodology' purposely expanded to explicitly address biostatistical considerations
Author: United States. Congress. House. Committee on Appropriations. Subcommittee on the Departments of Labor, Health and Human Services, Education, and Related Agencies
Publisher:
ISBN:
Category : Political Science
Languages : en
Pages : 1284
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Book Description
Author: John I. Gallin
Publisher: Academic Press
ISBN: 0123821673
Category : Medical
Languages : en
Pages : 798
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Book Description
This expanded third edition provides an introduction to the conduct of clinical research as well as more comprehensive and expansive content about the infrastructure necessary for a successful clinical research organization or enterprise. With authors who are experts in clinical research in both the public and private sectors, this publication provides essential information to clinical investigators who wish to develop and conduct well designed patient-based research protocols that comply with rigorous study design, ethical, and regulatory requirements.
