Recorded Webinar - Special Considerations in Pediatric Trials

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Recorded Webinar - Special Considerations in Pediatric Trials

$69.00

To purchase access for your team, or if you have any questions email us at info@clinicalpathwaysresearch.com.

A recording if the webinar will be available to attendees for 10 days. ONE license per purchase.

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Description:

This Special Considerations in Pediatric Clinical Trials recorded webinar covers highlights in pediatric clinical research legislation, physiological and developmental differences between children and adults, unique study procedure issues in pediatric populations, IRB review- informed consent: permission and assenting, and enrollment issues in pediatric studies. Includes important resources available to download from the recording.

Course Length: 90 minutes

Learning Objectives:

  1. Discuss a brief history of pediatric clinical trial legislation.

  2. Understand key physiological/developmental differences between children and adults.

  3. Discuss considerations in protocol design when developing a pediatric clinical trial.

  4. Understand the unique IRB review processes and consenting issues encountered in pediatric trials.

  5. Understand enrollment challenges and potential ways to work with these challenges.

Speaker:

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CHARLES "CHUCK" SATHER, BSN, CCRA

Charles "Chuck" Sather’s current focus of consulting is to promote efficiency in remote and on-site Monitoring and Auditing in a balanced, fair, and amiable manner. He has over 30 years of clinical experience with a Bachelor of Science Degree in Nursing and has been certified by the Association for Clinical Research Professionals (ACRP) as a CCRA for approximately 15 years. He is a frequent speaker at industry conferences, has authored multiple courses for clinical research training programs in various functional areas, and has been an Item Writer on ACRP’s Exam Committee.

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