Good Clinical Practice (GCP) in Clinical Research Suchart Chongprasert, Ph.D. Food And Drug Administration ICH GCP for Clinical Research investigators,
INTERNATIONAL ETHICAL GUIDELINES: CIOMS Robert J. Levine, MD Director: Donaghue Initiative in Biomedical and Behavioral Research Ethics; Professor of Medicine;
Research Ethics: The Protection of Human Subjects The Regulations and the Roles of the Researcher and the IRB Presented by Sinclair Community College Institutional.
AN OVERVIEW OF THE IRB Georgia Tech Office of Research Integrity Assurance.
Free, Prior and Informed Consent: A Right of Communities
What makes research ethical? 6. Informed consent cont’d Researchers can promote participants’ freedom by: –Adequate assessment of the specific vulnerability.
INTERNATIONAL ETHICAL GUIDELINES: CIOMS