Date: May 15, 2017
Time: 1pm - 2:30pm EST
Duration: 90 Minutes - Online
Sponsored by Life Science Training Institute
Pediatric clinical trials present unique challenges since minors, as a vulnerable population, require a variety of regulatory protections to be incorporated as part of the study’s design, recruitment strategies, and monitoring plan. In this session, a variety of strategies to ensure success when enrolling pediatric populations will be discussed. Join our own Charles “Chuck” Sather in this interactive presentation.
This session will use a 3-prong approach evaluating historical, scientific, and regulatory information to help better understand the special considerations encountered when enrolling minors in a study.
Take home benefits from this session will include:
- A discussion regarding the physiological and developmental differences between various pediatric populations as compared to adults
- Understanding of the Informed Consent/Permission and Assent in various pediatric populations
- Discuss enrollment issues and how parent perception can impact on enrollment
For more information, contact SAM at firstname.lastname@example.org.
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