How can smart authoring revolutionize your regulatory documentation?

 

Join our panel of experts from RQM+ and Fern.ai as they delve into the transformative benefits of structured content authoring. From reducing errors to enhancing efficiency, this discussion offers actionable insights for both regulators and manufacturers.

Discover how leaders like Celeste Maksim, Jaishankar Kutty, Jon Gimbel, Niki Spaniel, Margot Borgel and Alexia Haralambous leverage smart authoring to streamline processes and maintain compliance with evolving legislation like EU MDR 2017/745 and EU IVDR 2017/746.

Whether you're a seasoned professional or new to the MedTech field, this session will equip you with the knowledge to optimize your documentation strategies.

Discover how Fern.ai digitalizes and automates the clinical evaluation of medical devices:

Four key innovation drivers enabled by EU MDR

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Driver 1:

Clinical evaluation
workflow automation

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Driver 3:

Systematic post-market
surveillance

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Driver 2:

Streamlined external
collaboration

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Driver 4:

Cross-functional
knowledge sharing

Take a sneak peek

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