To participate in health research, there is a need for well‐administered informed consent.
Understanding of informed consent, especially in international health research, is influenced …

Informed consent is universally recognized as a central component of ethical conduct in
scientific research. Investigators working with diverse populations throughout the world face …

Background: The doctrine of informed consent (IC) exists to protect individuals from
exploitation or harm. This study into IC was carried out to investigate how different …

BY CHRISTINE PACE, EZEKIEL J. EMANUEL, THESHINEE CHUENYAM, CHRIS
DUNCOMBE, JUDITH D. BEBCHUK, DAVID WENDLER, JORGE A. TAVEL, LAURA A …

Informed consent is a basic requirement for the conduct of ethical research involving human
subjects. Currently, the Helsinki Declaration of the World Medical Association and the …

Although a relatively recent phenomenon, the role of informed consent in human research is
central to its ethical regulation and conduct. However, guidelines often recommend …

Ethical dilemmas in biomedical research, especially in vulnerable populations, often spark
heated debate. Despite recommendations and guidelines, many issues remain …

Obtaining 'informed consent'from every individual participant involved in health research is a
mandatory ethical practice. Informed consent is a process whereby potential participants are …

A major requirement for the ethical conduct of research, involving human subjects, is the
informed consent of the potential participant. Potential participants recruited should have …

Background Informed consent is often cited as the “cornerstone” of research ethics. Its intent
is that participants enter research voluntarily, with an understanding of what their …