Ethical Considerations When Preparing a Clinical Research Protocol Book

Ethical Considerations When Preparing a Clinical Research Protocol


  • Author : Evan DeRenzo
  • Publisher : Academic Press
  • Release Date : 2020-06-12
  • Genre: Medical
  • Pages : 370
  • ISBN 10 : 9780123869548
  • Total Read : 78
  • File Size : 17,8 Mb

DOWNLOAD BOOK
Ethical Considerations When Preparing a Clinical Research Protocol 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 Book

Ethical Considerations When Preparing a Clinical Research Protocol


  • Author : Evan DeRenzo
  • Publisher : Academic Press
  • Release Date : 2020-06-25
  • Genre: Medical
  • Pages : 368
  • ISBN 10 : 9780123869357
  • Total Read : 79
  • File Size : 17,8 Mb

DOWNLOAD BOOK
Ethical Considerations When Preparing a Clinical Research Protocol 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 Conduct of Clinical Research Involving Children Book

Ethical Conduct of Clinical Research Involving Children


  • Author : Institute of Medicine
  • Publisher : National Academies Press
  • Release Date : 2004-07-09
  • Genre: Medical
  • Pages : 445
  • ISBN 10 : 0309133386
  • Total Read : 70
  • File Size : 17,9 Mb

DOWNLOAD BOOK
Ethical Conduct of Clinical Research Involving Children Summary:

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.

Field Trials of Health Interventions Book

Field Trials of Health Interventions


  • Author : Peter G. Smith
  • Publisher : Oxford University Press, USA
  • Release Date : 2015
  • Genre: Medical
  • Pages : 479
  • ISBN 10 : 9780198732860
  • Total Read : 75
  • File Size : 20,5 Mb

DOWNLOAD BOOK
Field Trials of Health Interventions Summary:

"IEA, International Epidemiological Association, Welcome Trust."

Randomized Controlled Trials Book

Randomized Controlled Trials


  • Author : Phyllis Solomon
  • Publisher : Oxford University Press
  • Release Date : 2009-02-02
  • Genre: Social Science
  • Pages : 224
  • ISBN 10 : 0199715548
  • Total Read : 84
  • File Size : 5,8 Mb

DOWNLOAD BOOK
Randomized Controlled Trials Summary:

Randomized controlled trials (RCTs) are considered by many researchers and providers to be the gold standard of health and social service effectiveness research. However, there exist scant resources that deal with the complex nature of designing and implementing RCTs in community-based settings. This clearly written pocket guide provides researchers and social service practitioners insight into each step of an RCT. The goal of this text is to enable readers to understand, design, and implement a community-based RCT. From the initial stage of planning the RCT and developing its conceptual foundations through implementation, the authors provide a wealth of detail and case studies from social work practice research that assist readers to comprehend the detailed information provided. Accessible, concrete advice is woven throughout the text and tackles the many design and implementation challenges that arise in community practice settings. The importance of utilizing a mix of qualitative and quantitative methods is encouraged due to the intricate nature of RCT research in community-based environments. Through utilizing practical case examples, this pocket guide reviews the essentials of RCTs in a manner that will appeal to researchers, practitioners and students alike who are seeking the necessary tools to build the empirical knowledge base for community-based psychosocial interventions for social work.

The Belmont report Book

The Belmont report


  • Author : United States. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research
  • Publisher : Unknown
  • Release Date : 1978
  • Genre: Uncategoriezed
  • Pages : null
  • ISBN 10 : IND:30000050596992
  • Total Read : 65
  • File Size : 14,7 Mb

DOWNLOAD BOOK
The Belmont report Summary:

Reviewing Clinical Trials Book

Reviewing Clinical Trials


  • Author : Chinese University of Hong Kong
  • Publisher : Unknown
  • Release Date : 2010
  • Genre: Clinical trials
  • Pages : 153
  • ISBN 10 : 9881904110
  • Total Read : 91
  • File Size : 16,6 Mb

DOWNLOAD BOOK
Reviewing Clinical Trials Summary:

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 any way interfered with the project, except for providing nonbinding comments to the final product. The entire text of this manual was written by Johan PE Karlberg. Marjorie A Speers provided considerable and essential comments on the contents and the first and subsequent drafts. A group of international human research protection experts mostly working in non-profit institutions or organisations - see Contributors for details - reviewed and provided important comments on the contents and final draft. It was solely created with the intention to promote human research protection of participants in clinical trials. This manual will be translated into numerous languages and is provided free of charge as an electronic file over the Internet (http://www.ClinicalTrialMagnifier.com) and offered in print for a fee. The objective beyond this project is to establish educational activities, developed around the manual, and jointly organised with leading academic institutions worldwide.