DIA 2022 Global Annual Meeting

Component Type: Workshop
Level: Intermediate

Non-traditional qualitative methods (e.g., longitudinal qualitative interviews) have the potential to generate in-depth insights that are valuable to support medical product development across the lifecycle and during regulatory review. This workshop will explore practical considerations for study design and implementation (including benefits considerations for preserving clinical trial data integrity). Perspectives from research experts, regulatory, and patient representatives will be shared and key working models will be explored through case studies. Polling questions will help facilitate audience participation and inquiry.

Learning Objectives

Explore the use of non-traditional qualitative methods to inform regulatory review; Discuss best practices and key considerations for designing and implementing longitudinal qualitative research (LQR) in clinical trials; Explore patient, industry, and research expert perspectives on practical LQR study design and feasibility considerations.

Chair

Ebony Dashiell-Aje, PhD