Implementing and Managing a connected PMS program throughout your product lifecycle

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