Regulatory Open Forum

👋 Join us on November 30 at 11:00 am PST for a live #webinar with Victoria Samonte, M.D. from Abbott, David Kovac from DistillerSR and moderated by Michelle Zaharik, form MLZ Biotech Consulting.

The three will be discussing the challenges and opportunities related to #software implementation and #clinicalevidence management for medical devices.

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.

Who Should Attend?
-Regulatory Affairs Professionals
-Medical Affairs Professionals
-Quality Assurance Professionals
-Medical Writers
-Clinical Evaluation Managers
-Notified Bodies Representatives

You can register here: Western Canada Chapter Virtual Event: Automation and Literature Review Software Adoption Driving Confident IVDR Regulatory Submissions

Raps		remove preview
Western Canada Chapter Virtual Event: Automation and Literature Review Software Adoption Driving Confident IVDR Regulatory Submissions Timely and compliant submissions remains a challenge for global medical device companies. Rejected submissions result in unforeseen costs and negatively impact planned product launches and device market availability. View this on Raps >