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Evaluation On-Demand Video

2024 PRIM&R Annual Conference

Pharma/Biotech Perspectives

Informed Consent

Research Involving Data and New Technologies

IRB Review

B04 - Ethical Implications and Practical Application of Broad Consent

Monday, November 18, 2024
1:45 PM – 3:00 PM PT
Location: Room 343-344
Live Session Recorded Human Subject Research - HSR Call for Session Proposal - CSP Deep Dive Series CIP Accredited
CLICK HERE to view captioning for this session! 

Broad consent allows researchers to conduct research on identifiable data/biospecimens without study specific consent or having to request a waiver of informed consent. This reduces administrative burden on researchers sharing data and specimens and for using these materials in future research. This session will explore the benefits and ethical implications of broad consent as well as the operational challenges that institutions face when implementing it.

Learning Objectives:

  • Identify the operational infrastructure needed to implement broad consent at an institution
  • Obtain an understanding of operational models that can be used to facilitate broad consent
  • Articulate ethical concerns associated with broad consent
  • Evaluate the perspectives and opinions that research participants and member of the public hold regarding broad consent