5/29/2018

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

Sign up here

Description:

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

Enjoy this blog? Please like, comment, and share with your contacts.