Transforming Medical Writing: The Role of AI in Innovation
AI's Impact on Regulatory Medical Writing
In today's rapidly evolving healthcare landscape, the integration of artificial intelligence (AI) is significantly altering the dynamics of regulatory medical writing. This free webinar offers an intriguing opportunity to explore how AI can complement the essential skills of medical writing teams, enhancing their capabilities and effectiveness. Attendees will gain invaluable insights into the benefits of utilizing AI as a powerful co-pilot in the writing process, thereby increasing productivity and allowing writers to focus on higher-value tasks.
The Co-Pilot Concept in Medical Writing
AI is not here to take over the role of medical writers; rather, it serves as a valuable partner, enabling them to excel in their work. This session will challenge the prevailing myth that AI threatens the jobs of experienced regulatory writers. Instead, participants will learn how AI enhances their strategic impact and efficiency, ultimately improving the quality of medical writing submissions.
Shifting Roles of Medical Writers
As AI becomes an integral tool in regulatory writing, the role of medical writers is evolving. Writers are transitioning from merely producing content to overseeing, analyzing, and validating information. This shift necessitates a new skill set, with writers becoming proficient in guiding AI to transform complex data into coherent narratives while ensuring data integrity.
Practical Use Cases for AI
This informative session will showcase real-world applications of AI that are reshaping workflows and accelerating project timelines. Some highlighted use cases include:
- Creating informed consent forms
- Preparing clinical study reports
- Simplifying lay summaries for diverse audiences
- Enhancing review and quality control processes across all regulatory writing tasks
Navigating Change Management
The introduction of AI into regulatory writing requires careful planning. This webinar will delve into essential change management strategies to help teams adapt to new technologies confidently. Key topics will include fostering an environment of psychological safety, designing effective upskilling programs, and establishing governance protocols related to AI use.
Empowering Medical Writing Teams
Through thoughtful implementation of AI tools, organizations can significantly reduce submission timelines, facilitating faster market access for crucial therapies. This session is especially relevant for leaders dedicated to empowering their medical writing teams, ensuring they remain at the forefront of excellence while leveraging AI as a supportive tool.
Expert speakers from the PPD Clinical Research Business of Thermo Fisher Scientific, including Maria Hopfgarten, Head of Global Medical Writing, and Sarah Frost, Functional Service Partnership (FSP) Lead for Medical Writing, will share their insights in this live webinar.
Join the Discussion
Mark your calendars for this enlightening webinar broadcast. Engage with industry experts as they explore the balance between innovation and human expertise in regulatory medical writing.
Frequently Asked Questions
What is the main focus of the webinar?
The webinar will explore the role of AI in enhancing the skills of medical writers and improving regulatory writing processes.
How can AI support medical writers?
AI acts as a co-pilot, enhancing productivity, strategic impact, and the capacity for complex problem-solving.
What are some use cases of AI in medical writing?
Use cases include informed consent forms, clinical study reports, lay summaries, and quality control for submissions.
Who are the speakers in this webinar?
Maria Hopfgarten and Sarah Frost, experts from PPD Clinical Research Business of Thermo Fisher Scientific, will lead the session.
What strategies will be discussed for adapting to AI?
The webinar will address change management strategies, including training programs and governance around AI usage.
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