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Improving the Informed Consent Process
Session Chair(s)
Kathleen Findlen
Head of Clinical Operations and Project Management, Piramal Life Sciences, United States
Research Consent in Acute Settings: What Works?
Learning Objective : Provide practical, clear, and concise guidelines that clinical trial personnel can use to decide when they could include subjects who cannot consent in a clinical trial; Describe three solutions to obtaining appropriate informed consent from potential participants who are in an acute health care setting; Discuss methods and strategies to improve comprehension of informed consent in clinical trials.
Speaker(s)
Mitchell Parrish, JD, RAC
President, H Clinical, United States
Research Consent in Acute Settings: What Works?
Ricardo Nunez, DrMed
Director, Medical. Central Nervous System., Quintiles Inc., United States
Can Subjects Who Cannot Sign Informed Consent Be Enrolled in My Trial?
Brenda Jamerson, PHARMD
Center Fellow, Biobehavioral and Social Aspects of Health Disparities, Duke University, United States
Strategies to Improve the Informed Consent Process to Enhance Comprehension and Recruitment of Ethnically Diverse Populations
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