Writing Clinical Research Protocols - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Writing Clinical Research Protocols write by Evan G. DeRenzo. This book was released on 2006. Writing Clinical Research Protocols available in PDF, EPUB and Kindle. 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 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 will be 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
Writing Clinical Research Protocols
Writing Clinical Research Protocols - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Writing Clinical Research Protocols write by Evan DeRenzo. This book was released on 2005-09-08. Writing Clinical Research Protocols available in PDF, EPUB and Kindle. 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
Writing Your First Clinical Research Protocol
Writing Your First Clinical Research Protocol - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Writing Your First Clinical Research Protocol write by Colleen Aldous. This book was released on 2011-09-01. Writing Your First Clinical Research Protocol available in PDF, EPUB and Kindle. Students embarking on their first clinical research protocol are often daunted by the task at hand, particularly by the statistical terminology, concepts and the choice of appropriate statistical tests. The authors understand the difficulties and pitfalls students might encounter and have written an introductory text that will make writing that first protocol 'a breeze'. Beginning with a section entitled 'Whats in it for me', which outlines the benefits of research, the text provides ideas and advice on topics such as finding the research focus, writing the proposal, considering ethical requirements, compiling a budget and writing the executive summary.
The Clinical Trial Protocol
The Clinical Trial Protocol - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook The Clinical Trial Protocol write by Sue Fitzpatrick. This book was released on 2005-12. The Clinical Trial Protocol available in PDF, EPUB and Kindle.
Ethical Considerations When Preparing a Clinical Research Protocol
Ethical Considerations When Preparing a Clinical Research Protocol - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Ethical Considerations When Preparing a Clinical Research Protocol write by Evan DeRenzo. This book was released on 2020-06-25. Ethical Considerations When Preparing a Clinical Research Protocol available in PDF, EPUB and Kindle. 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
