Healthcare companies such as medical device manufacturers and pharma/biotech companies have a regulatory and legal obligation to convert key scientific content into plain language for lay audience consumption around the world. From producing clinical trial lay summaries for the general public to the action-focused informational content generation aimed at the Health Care Provider (HCP) audience, the need to produce a multitude of plain language written deliverables has strained many already-stretched internal teams. How can your organization meet these challenges?
Who is this webinar for?
Those Regulatory, Quality and Clinical leaders and teams who are tasked with the development, writing, review, or approval of medical device or pharmaceutical communications.
|February 8, 2023||Watch at a Convenient Time||Recorded|
Takeaways from this session:
Understand key aspects and the regulatory/legal aspects that define plain language writing
Learn how to tailor plain language writing for multiple audiences, e.g., lay audience versus Health Care Providers (HCPs)
Discuss how to standardize key messaging across multiple written deliverables and platforms