Textbook Of Clinical Research Ethics by Ezekiel J Emanuel (Editor)
- Publisher: MEDICAL BOOKS
- Availability: In Stock
- SKU: 46847
- Number of Pages: 827
Rs.1,620.00
Rs.2,095.00
Tags: best books , Best Price , Best Selling Books , Biomedical Research Ethics , Christine C Grady , Clinical Research Ethics , Clinical Trial Ethics , David D Wendler , Ethical Challenges in Medicine , Ethical Considerations in Human Trials , Ethical Decision Making , Ethical Dilemmas in Research , Ethical Frameworks in Medicine , Ethical Issues in Clinical Trials , Ethical Principles in Research , Ethical Review Process , Ethical Use of Placebos , Ethics in Drug Development , Ezekiel J Emanuel , Franklin G Miller , Good Clinical Practice (GCP) , Human Subject Research , Informed Consent , Institutional Review Board (IRB) , Medical Ethics , Medical Law and Ethics , Medical Research Guidelines , ONLINE BOOKS , Online Bookshop , Patient Rights in Research , Pharmaceutical Research Ethics , Public Health Ethics , Reidar K Lie , Research Ethics Guidelines , Research Misconduct , Research Regulations , Robert A Crouch , Scientific Integrity , Textbook Of Clinical Research Ethics
Textbook of Clinical Research Ethics
Editors: Ezekiel J. Emanuel, Christine C. Grady, Robert A. Crouch, Reidar K. Lie, Franklin G. Miller, David D. Wendler
Introduction
Textbook of Clinical Research Ethics is a comprehensive guide to the ethical principles and challenges involved in conducting clinical research. This book provides a multidisciplinary perspective, covering topics such as informed consent, risk-benefit analysis, research involving vulnerable populations, and international ethical guidelines. Designed for researchers, bioethicists, and policymakers, it offers practical insights and theoretical discussions to ensure ethical standards in medical and scientific research.
Key Points
1. Foundations of Clinical Research Ethics
- Explains the historical evolution of research ethics, including key ethical codes and regulations.
- Discusses the importance of ethical oversight in medical and clinical studies.
2. Informed Consent and Participant Rights
- Highlights the significance of voluntary and informed participation in research.
- Addresses challenges related to obtaining and ensuring valid informed consent.
3. Risk-Benefit Analysis in Research
- Explores methods for evaluating and balancing risks and benefits in clinical trials.
- Discusses ethical concerns related to experimental treatments and human subject protection.
4. Ethical Considerations in Global and Vulnerable Populations
- Examines the ethical challenges of conducting research in developing countries.
- Addresses the protection of vulnerable groups, including children, prisoners, and the mentally ill.
5. Ethical Review, Regulations, and Compliance
- Describes the role of Institutional Review Boards (IRBs) and ethical committees.
- Provides guidelines for ensuring compliance with international and national research ethics standards.
Why Read This Book?
- Essential for researchers, medical professionals, and bioethicists involved in clinical trials.
- Provides in-depth discussions on ethical issues with real-world case studies.
- Covers international guidelines, making it relevant for global research initiatives.
- Helps researchers navigate ethical dilemmas and ensure responsible conduct in clinical studies.
Conclusion
Textbook of Clinical Research Ethics is a vital resource for understanding and applying ethical principles in clinical research. By addressing theoretical and practical concerns, this book equips researchers with the knowledge needed to conduct studies responsibly while upholding the rights and safety of participants.