Webinar Recording: Automation and Literature Review Software Adoption Driving Confident Regulatory Submissions
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.
Watch the Webinar
Emily Metcalfe, MSc, RAC
Senior Manager, Clinical Product Risk at Boston Scientific
Camie Meichsne Meller, PhD, MS, BCMAS
Senior Manager of Clinical Evidence at BD
Director Clinical Affairs Trauma at Stryker
SVP, Strategic Growth at DistillerSR
Dr. Bassil Akra
Founder & CEO AKRA Team GmbH