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Join us for an engaging discussion where medical device regulatory subject matter experts will explore tools and strategies to streamline benefit-risk calculations under the EU MDR framework.
This webinar will provide practical guidance on calculating both qualitative and quantitative benefit-risk profiles, helping you avoid non-conformances and deliver compliant, data-driven submissions.
Through real-world case studies, our experts will demonstrate how to streamline the assessment process and present measurable outcomes that stand up to regulatory scrutiny. Whether you’re involved in regulatory submissions or product development, this session will give you the tools you need to navigate the EU MDR’s rigorous benefit-risk requirements.
Don’t miss this opportunity to enhance your regulatory skills and understanding.
Gain actionable knowledge and insights with our webinar:
Online Webinar
March 12, 2025 | 10:00 AM ET
Senior Manager, Medical Device Services, Celegence
Team Lead, Medical Device Services, Celegence
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