Plain language regulatory requirements have recently come into effect for the EU and UK. This webcast will provide an overview of both the regulations and guidance around plain language summaries (PLS) and other documents. The webcast will also look at the “why” behind plain language regulations and how they can be used for patient engagement and to increase clinical trial health literacy.
Learning Objectives
- Understand the changing regulations and industry trends impacting PLS
- Recognize the importance of PLS and other documents from a public health perspective
- Learn how PLS can be used to increase patient engagement
Audience Learning Level
Basic: Content is introductory in nature and requires no requisite knowledge or experience to grasp concepts and related exercises. Basic educational activities are meant to establish a foundation of knowledge and/or competence that will be expanded upon in practice or in higher level activities.
Who Should Attend?
- Regulatory professionals who work in clinical trials
- Those interested in patient engagement and health literacy
