Ethical Considerations When Preparing a Clinical Research Protocol
  • Author : Evan DeRenzo
  • Release Date : 12 June 2020
  • Publisher : Academic Press
  • Genre : Medical
  • Pages : 370
  • ISBN 13 : 9780123869548

Ethical Considerations When Preparing a Clinical Research Protocol Book Summary

Ethical Considerations When Preparing a Clinical Research Protocol, Second Edition, provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. It includes practical information on ethical principles in clinical research, how to design appropriate research studies, how to consent and assent documents, how to get protocols approved, special populations, confidentiality issues, and the reporting of adverse events. The book's valuable appendix includes a listing of web resources about research ethics, along with a glossary, making it an invaluable resource for scientists collaborating in clinical trials, physician investigators, clinical research fellows, and more. Walks investigators and trainees through the identification of the ethical aspects of each section of a clinical research protocol Includes case histories that illustrate key points Contains information on conducting clinical research within the pharmaceutical industry Includes internet resources and worldwide web addresses for important research ethics documents and regulations Contains a chapter on Study Design and Methodology that is purposely expanded to explicitly address biostatistical considerations

Ethical Considerations When Preparing a Clinical Research Protocol

Ethical Considerations When Preparing a Clinical Research Protocol

Author : Evan DeRenzo,Eric A. Singer,Joel Moss
Publisher : Academic Press
Genre : Medical
Total View : 5351 Views
File Size : 42,9 Mb
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Ethical Considerations When Preparing a Clinical Research Protocol, Second Edition, provides a foundation for improving skills in the understanding of ethical requirements in the design and conduct of clinical research. It includes practical information on ethical principles in clinical research, how to design appropriate research studies, how to consent and ...

Writing Clinical Research Protocols

Writing Clinical Research Protocols

Author : Evan G. DeRenzo,Joel Moss
Publisher : Academic Press
Genre : Medical
Total View : 4320 Views
File Size : 47,5 Mb
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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. It includes practical information on ethical principles in clinical research, designing appropriate research studies, writing consent and assent documents, getting protocols approved, special ...

Field Trials of Health Interventions

Field Trials of Health Interventions

Author : Richard H. Morrow,David A. Ross
Publisher : Oxford University Press, USA
Genre : Tropical medicine
Total View : 5721 Views
File Size : 45,7 Mb
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Before new interventions can be used in disease control programmes, it is essential that they are carefully evaluated in "field trials", which may be complex and expensive undertakings. Descriptions of the detailed procedures and methods used in trials that have been conducted in the past have generally not been published. ...

Ethical Conduct of Clinical Research Involving Children

Ethical Conduct of Clinical Research Involving Children

Author : Institute of Medicine,Board on Health Sciences Policy,Committee on Clinical Research Involving Children
Publisher : National Academies Press
Genre : Medical
Total View : 2437 Views
File Size : 42,6 Mb
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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 ...

Reviewing Clinical Trials

Reviewing Clinical Trials

Author : Chinese University of Hong Kong,Chinese University of Hong Kong. Clinical Trials Centre,Washington, DC. Association for the Accreditation of Human research Protection Programs, Inc
Publisher : Unknown
Genre : Clinical trials
Total View : 1155 Views
File Size : 47,9 Mb
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The idea for this manual came from Pfizer in the US, which provided the Clinical Trials Centre at The University of Hong Kong, Hong Kong SAR, PR China with a nonbinding grant for its development. The general project layout protocol was accepted by Pfizer in July 2009. Pfizer has not in ...

Tri council Policy Statement

Tri council Policy Statement

Author : Anonim
Publisher : Unknown
Genre : Human experimentation in medicine
Total View : 1065 Views
File Size : 43,5 Mb
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This document is a joint policy of Canada's three federal research agencies, the Canadian Institutes of Health Research, the Natural Sciences and Engineering Research Council of Canada, and the Social Sciences and Humanities Research Council of Canada. This updated version replaces the TCPS 2 (2010) as the official human research ethics policy ...