Sponsored Webcast: Plain Language Summaries: Understanding the “Why” Behind the Regulations and Guidance (On Demand)
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.
Registration Fees & Deadlines
17 August 2023 – 18 October 2023: Free
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
Speaker
Lee Holland, PharmD, MPH
Certara, Associate Director – Regulatory Services Management – PLS
Lee Holland is the Associate Director, Regulatory Services Management of Plain Language Summaries at Certara. She has a decade of research and medical writing experience and has overseen the authoring of over 200 plain language documents.
