The Patient Role in Medicines Development [Video]

The complexity of modern clinical trials, the increasing importance of Real World Evidence (RWE) data, and the critical role of patient compliance with prescribed therapies underscore the significance of patient interaction in contemporary medicine development. Recognizing this, many Ethics Committees now include an “expert patient” among their members, who provides valuable, pragmatic insights into study design. Similarly, regulatory committees often feature representatives from patient organizations.

This evolving vision of patient involvement in medicine development represents a significant innovation, warranting focused discussion.

Learning Objectives for the Webinar:
Participants in this webinar will gain familiarity with:

-The emerging roles of “expert patients” and patient organizations in the field of medicine development.
-The key responsibilities assigned to these patients by National Ethics Committees and Regulatory Bodies.
-The training programs designed to educate patients on the critical elements of medicine development.