Tag Archive: Ethics

Regulatory & Ethics Support

The ICTR offers education, expert advice and resources to better equip study teams to conduct research that is ethical, relevant and responsive to the interests of patients and research participants. Clinical Research Billing Compliance (CRBC) ClinicalTrials.gov Program Office of Human Subjects Research (OHSR) & Johns Hopkins Medicine Institutional Review Boards (IRB) Research Ethics Consultation Clinical Research Support Services (CRSS) Drug and Device Resource Service (DDRS) Office of Research Administration (ORA) Research Participant Advocacy Program

4th Annual Trends in Clinical Research

Presentations: Jonathan Moreno, PhD Christopher Chute, MD, DrPh Kathi Huddleston, PhD, RN Nancy Kass, ScD  

Research Ethics Consultation

The Research Ethics Consultation Service helps to raise awareness of, and to assist investigators in resolving ethical issues throughout the entire research process. Consults may be requested for ethical issues arising during study development, conduct, analysis and publication. Our consultants offer ethical guidance on topics such as: Determining appropriate interventions and controls to include in studies; Maintaining confidentiality in recruitment; Using alternative approaches to informed consent; and Responding appropriately when an unforeseen event occurs during data collection. Note: The service is not designed to “pre-review” submissions to the IRB nor to review or draft consent documents. Research Ethics Consultation Service … Continue reading