I. Defining "research"--II. Issues in study design . -- III. Harm and benefit -- IV. Voluntary informed consent -- V. Standard of care -- VI. Obligations to participants and communities -- VII. Privacy and confidentiality -- VIII. Professional ethics.
This collection is envisioned principally as a tool to aid educational programs, from short workshops on research ethics to in-service learning for scientists and REC members, to formal degree or certificate courses.
This collection is envisioned principally as a tool to aid educational programs, from short workshops on research ethics to in-service learning for scientists and REC members, to formal degree or certificate courses.
No other volume has this scope. Students in bioethics, public and international health, and ethics will find this book particularly useful.
The central claim of this book is that ethics is an important common ground for all of the health professions.
This book is open access, which means that you have free and unlimited access. This book highlights the ethical issues and dilemmas that arise in the practice of public health.
This book is open access, which means that you have free and unlimited access. This book highlights the ethical issues and dilemmas that arise in the practice of public health.
Consult 2.6(b): Reason for Consult Daryl Saunders, a nurse manager, called to determine what the requirements are for informed consent for someone who is blind. Narrative Casey Wright, a blind research participant, is enrolled in ...
Casebook on benefit and harm
This book is open access, which means that you have free and unlimited access. This book highlights the ethical issues and dilemmas that arise in the practice of public health.
Bioethics and Public Health Law is based on Part II--The Patient, the Provider, and the State, of parent book Health Care Law and Ethics, and adds additional coverage a variety of issues and topics not covered in the parent book.