About This Webinar

In this webinar roundtable moderated by Dr. Bassil Akra from AKRA Team GmbH , Camie Meichsner Meller, Senior Manager of Clinical Evidence at BD, Arthur Ganz, Director, Clinical Affairs Trauma at Stryker, and Emily Metcalfe, Senior Manager, Clinical Product Risk at Boston Scientific discussed the challenges and opportunities related to software implementation and evidence management for medical devices leading to confident regulatory submissions.

Key Learning Objectives:

• Achieving confidence in regulatory submissions for a faster path to compliance.
• Assessing literature review data quality.
• Implementing continuous and efficient evidence management practices from pre-market approval through post-market surveillance.
• Leveraging standardized and repeatable organizational processes for audit-ready literature reviews.