[FREE WEBINAR] Developing Effective Patient-Focused Content: Writing Plain Language Lay Summaries and SSCP Patient Sections


Click here to watch the recording of this webinar.

Healthcare companies continually strive to communicate important information about their drugs and devices to diverse audiences comprised of patients, caregivers, healthcare professionals (HCPs), and the general public. The use of plain language written communication can help ensure key health information and clinical research findings are understandable and accessible to all. 
In this second presentation of our Deep-Dive: Plain Language Writing webinar series, we will focus on best practices that guide the development of common forms of plain language communication intended for the patient, their families and/or caregivers, such as the: 
• Patient section of an EU MDR-compliant Summary of Safety and Clinical Performance (SSCP) for all Class III and Active Implantable Medical Devices (AIMD) 
• Plain Language Summary (PLS) of a published journal article 
• Lay summaries required under EU CTR for clinical trials on medicinal products

Join us as we discuss practical strategies you can use to develop effective patient-centered lay summary content.

Who are the Panelists?

Laurie Mitchell, President of Criterion Edge.

Sign up for future webinars here.

Criterion Edge has the expertise and resources to write your clinical or performance evaluation report. Ready for a free consult?



Tags: , , ,

[Free Webinar] IVDR Readiness: Creating a Blueprint to Build a Strong PER

Join us on Wednesday, June 7th, 2023 at 11 AM PST, as our regulatory experts discuss the process of writing a PER, with careful attention to the importance of aligning technical documents to create a cohesive, well-organized report.

Spots are limited – click to register for this free webinar.

Check out our Events Calendar for our upcoming webinars.

Named the #1 Regulatory Services Company 2022 by Life Sciences Review