Date: June 4, 2018
Time: 1:00 p.m. – 2:30 p.m. EDT
Duration: 90 minutes
Sponsored by: Life Science Training Institute
Webinar: Live interactive session and recorded (available for 30 days)
Testing and completion certificate available
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Pediatric clinical trials present unique challenges for monitors and coordinators alike. 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.
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.
Key take away benefits:
- A discussion regarding the physiological and developmental differences between various pediatric populations as compared to adults (ADME)
- Discuss considerations in protocol design when developing a pediatric clinical trial
- Discuss enrollment issues and how parent perception can impact on enrollment
-The Clinical Pathways Team
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