Challenges & Solutions: Designing ePRO And eConsent For Pediatric Trials

Pediatric studies present unique data collection challenges that require careful attention. In this webinar, we explore how enhancing the trial experience for child participants and their parents can alleviate their burdens and improve the quality and reliability of the data collected.

Gain confidence in making your next pediatric trial more successful by leveraging the technology discussed to address common challenges in pediatric studies.

What We Discussed:

• The challenges faced by "clinical trial families"
• Strategies to overcome enrollment and retention friction points
• Navigating 21 CFR Part 11 compliance issues
• Effective approaches for working with children under 13
• Meeting state and international regulatory requirements
• Multi-user workflows and more!

Key Takeaways:

• Pediatric studies demand solutions that ease the study process for participants and their families.
• Technology is crucial in simplifying logistics, offering flexibility, and ensuring a smooth experience for pediatric trial participants.
• Informed consent requires age-appropriate communication and active parental involvement.
• Compliance with privacy, auditability, and 21 CFR Part 11 involves careful use of electronic signatures, audit trails, and authentication methods.
• Managing young participants effectively necessitates age-appropriate content, flexibility, and personalized experiences.

Watch our on-demand webinar below where guest speaker Gauri Nagrani shares insights on enhancing the quality, speed, and user experience of pediatric clinical trials. This presentation is valuable for sponsors, investigators, and study teams looking to refine their approach to pediatric studies.