Webinar Recording: Automation and Literature Review Software Adoption Driving Confident Regulatory Submissions

The webinar is over but you can watch it on demand.

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.
Duration: 1 Hour

Watch the Webinar

Speakers
Emily Metcalfe, MSc, RAC

Emily Metcalfe, MSc, RAC

Senior Manager, Clinical Product Risk at Boston Scientific

Camie Meichsne Meller, PhD, MS, BCMAS

Camie Meichsne Meller, PhD, MS, BCMAS

Senior Manager of Clinical Evidence at BD

Arthur Ganz

Arthur Ganz

Director Clinical Affairs Trauma at Stryker

Marc Dufresne

Marc Dufresne

SVP, Strategic Growth at DistillerSR

Dr. Bassil Akra

Dr. Bassil Akra

Founder & CEO AKRA Team GmbH