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PRODID:-//UIC
BEGIN:VEVENT
UID:2026040509202320250425T12000020250425T13000069d2d21712047@uic.edu
CATEGORIES:MEETING
STATUS:TENTATIVE
DTSTAMP:20250331T104640
DTSTART:20250425T120000
DTEND:20250425T130000
SUMMARY:Informed Consent for Vulnerable Populations in Clinical Research: Balancing Protection, Access, and Equity
DESCRIPTION:  Description:   This talk explores the ethical and regulatory challenges of obtaining informed consent from vulnerable populations in clinical trials. It will discuss strategies to ensure ethical enrollment while balancing the need for scientific rigor, equitable access to research, and participant protection. Attendees will gain insights into regulatory frameworks, risk-benefit considerations, and best practices for fostering inclusivity in clinical research.  Speakers:   Ryan Nguyen, DO  Assistant Professor of Clinical Medicine  Precision Oncology Program Lead    &    Meredith Russell, BS, CCRP  Associate Director of Clinical Research Operations, Clinical Trials Office  University of Illinois Cancer Center    \n    Clinical Research Investigators Seminar Series (CRISS): This training seminar series is intended to provide faculty and other investigators with information and skills needed to conduct clinical research at UIC at all stages of a study?s lifecycle.    \n      Register  | Event post: https://ahs.uic.edu/inside-ahs/events?page_id=26013
LOCATION:    Select 
CLASS:PRIVATE
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