Clinical trials in brain tumours- What you always wanted to know but were afraid to ask Zarnie Lwin Department of Medical Oncology, Mater Adult Hospital.
Ethical Issues Raised by Current Research on Drug Addiction Dr Tom Walker Centre for Professional Ethics Keele University United Kingdom.
Ethical Legal/Issues in Human Subject Research II ISD II – Infectious Diseases Barbara Barrowman Andrew Latus March 7, 2003.
Ethical Decision-Making in Pediatrics Holly K. Tabor, Ph.D. Assistant Professor Department of Pediatrics University of Washington Treuman Katz Center for.
“Good Clinical Practices” in Meeting Regulatory Responsibilities Terry VandenBosch, RN, PhD, CIP, CCRP Senior Research Compliance Associate Office of Human.
Determining capacity and protecting subjects who have lost capacity Jason Karlawish, MD University of Pennsylvania.
Pre-randomisation consent (Zelen’s method). Background Most individually randomised trials ask patient CONSENT before randomisation. There are problems.
What makes research ethical? 6. Informed consent cont’d Researchers can promote participants’ freedom by: –Adequate assessment of the specific vulnerability.
Legislation in the ED Peer Support 27_01_2015 Sophie Rozwadowski & Kate Myler.
Informed Consent: Requirements
+ Approaches to consent in children’s emergency care: CONNECT study guidance development @CONNECTStudy.
Consenting for Planet-2