Simplifying Systematic Literature Reviews: Overcoming Regulatory Challenges with Automation and GenAI
- When: March 18, 2025 | 10:00 AM EST
- Where: Online Webinar
- How to Register: Sign up
Webinar Overview
Successfully completing systematic literature reviews (SLRs) for medical devices is a complex, time-consuming process. Regulatory requirements demand thorough searches across thousands of articles, precise data extraction, and structured reporting – all of which can slow down submissions and increase resource costs.
Traditional manual methods often lead to inefficiencies, delays, and compliance risks. But with the right technology, SLRs can be faster, more accurate, and fully aligned with evolving regulatory expectations.
Join Celegence’s webinar to learn how automation and GenAI-powered tools like CAPTIS® are transforming the SLR process – helping medical device manufacturers improve efficiency, reduce manual effort, and ensure compliance with regulatory bodies.
What You’ll Learn
This webinar is designed for regulatory professionals, medical writers, and quality teams looking to enhance their SLR workflows with technology-driven solutions.
Key takeaways include
- The Critical Role of SLRs: Why systematic literature reviews are essential for regulatory submissions and compliance.
- Addressing Notified Body Expectations: Learn how to align your LSR documentation with evolving regulatory standards.
- Technology-Driven Efficiency: Discover how automation and GenAI tools, like CAPTIS®, can improve efficiency, accuracy, and compliance.
- Overcoming Common Challenges: Get expert strategies to tackle data management, documentation accuracy, and workflow optimization.
- Practical Solutions for Medical Device Manufacturers: Actionable tips for reducing manual effort while ensuring regulatory compliance.
Who Should Attend?
This session is tailored for professionals in the medical device sector who are responsible for regulatory compliance, literature reviews, and quality documentation, including:
- Regulatory professionals managing literature reviews for clinical evaluations and technical documentation.
- Medical writers and quality teams looking to improve their SLR processes.
- Medical device manufacturers seeking faster, more efficient, and compliant literature reviews.
Don’t miss this opportunity to simplify your SLR workflows with AI-driven technology. Register now!
Meet the Experts
Why You Can’t Miss This Webinar
- Practical Strategies: Learn from real-world case studies and expert insights.
- Technology-Enabled Efficiency: Discover how automation and GenAI tools can optimize regulatory workflows.
- Exclusive Expert Q&A: Have your most pressing regulatory questions answered live.
- Recording Available: Can’t attend live? Register now and receive the recording after the session.
🔗 Don’t miss out—secure your spot today! Register Now
