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 …

The informed consent process has become a universal requirement for research involving
human subjects. Its goal is to inform volunteers regarding research in order to make decision …

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 …

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 …

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

Objective Some researchers claim that the quality of informed consent of clinical research
participants in developing countries is worse than in developed countries. To evaluate this …

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 …

This report is a summary of presentations and discussions at a seminar entitled “Informed
Consent: From Good Intentions to Sound Practices.” This two-day seminar brought together …

e attitudes and practices of investigators who engage in the process of obtaining informed
consent from research subjects are central both to understanding how informed consent is …