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;
What makes research ethical? 6. Informed consent cont’d Researchers can promote participants’ freedom by: –Adequate assessment of the specific vulnerability.
Research Ethics: The Protection of Human Subjects The Regulations and the Roles of the Researcher and the IRB Presented by Sinclair Community College Institutional.
INTERNATIONAL ETHICAL GUIDELINES: CIOMS
AN OVERVIEW OF THE IRB Georgia Tech Office of Research Integrity Assurance.
Free, Prior and Informed Consent: A Right of Communities
