Implementing and Managing a connected post-market surveillance program throughout your product lifecycle

Galen Data Medical Device Innovation Webinar Series Presents:   

IMPLEMENTING AND MANAGING A CONNECTED POST-MARKET SURVEILLANCE PROGRAM THROUGHOUT YOUR PRODUCT LIFECYCLE  

Description: While often thought of as a burdensome regulatory activity, post-market surveillance requires full adoption across the product lifecycle– including quality, regulatory, product development, and clinical teams. With the adoption of the EU MDR and increased focus on device safety reporting by the US FDA,  the emphasis on post-market surveillance has never been stronger.  Join Galen Data and Greenlight Guru, in discussing the foundation of post-market surveillance (PMS) and learn best practices to ensure that devices continue to be safe and effective. Whether you’re pre-market and looking to build out a post-market surveillance program for the first time, or want to make improvements to your current program, it’s never too early (or late) to begin and update your PMS.   

Key Takeaways:  

👉 Understand the regulatory requirements for post-market surveillance for quality, regulatory, product development, and clinical teams 

👉 Discover how to incorporate connectivity to streamline post-market surveillance 

👉 Uncover best practices for post-market surveillance  

Speakers:  

Jon I. Bergsteinsson, Co-founder of SMART-TRIAL by Greenlight Guru 

Brittani Smith, Medical Device Guru at Greenlight Guru