The perspectives of researchers on obtaining informed consent in developing countries

SK Newton, J APPIAH‐POKU - Developing World Bioethics, 2007 - Wiley Online Library
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 …

Informed consent in human subject research: a comparison of current international and Nigerian guidelines

JO Fadare, C Porteri - Journal of Empirical Research on …, 2010 - journals.sagepub.com
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 …

Informed consent: From good intentions to sound practices—A report of a seminar

SY Wood, B Friedland, CE McGrory - 2002 - knowledgecommons.popcouncil.org
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 …

[PDF][PDF] Informed consent of human subjects: A review

MR Islam - Bangladesh Journal of Bioethics, 2014 - pdfs.semanticscholar.org
Informed consent is a vital part of the research process, and as such entails more than
obtaining a signature on the consent form. Researchers or investigators must educate …

Understanding informed consent for participation in international health research

AS Jegede - Developing world bioethics, 2009 - Wiley Online Library
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 in health research: Challenges and barriers in low‐and middle‐income countries with specific reference to Nepal

PR Regmi, N Aryal, O Kurmi, PR Pant… - Developing world …, 2017 - Wiley Online Library
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 …

[HTML][HTML] Researchers' views on, and experiences with, the requirement to obtain informed consent in research involving human participants: a qualitative study

A Xu, MT Baysari, SL Stocker, LJ Leow, RO Day… - BMC medical …, 2020 - Springer
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 …

Module two: informed consent

P Andanda - Developing World Bioethics, 2005 - Wiley Online Library
MODULE TWO: INFORMED CONSENT Page 1 © Blackwell Publishing Ltd. 2005, 9600
Garsington Road, Oxford OX4 2DQ, UK and 350 Main Street, Malden, MA 02148, USA …

[HTML][HTML] Informed consent in an African context

C Wasunna, J Tegli, P Ndebele - … ethics in Africa: A resource for …, 2014 - books.google.com
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 …

The quality of informed consent in a clinical research study in Thailand

C Pace, EJ Emanuel, T Chuenyam, C Duncombe… - IRB: Ethics & Human …, 2005 - JSTOR
BY CHRISTINE PACE, EZEKIEL J. EMANUEL, THESHINEE CHUENYAM, CHRIS
DUNCOMBE, JUDITH D. BEBCHUK, DAVID WENDLER, JORGE A. TAVEL, LAURA A …