Running the QMSR Gambit: Impacts to Medical Devices and Combination Products

When:  Jun 25, 2024 from 12:00 PM to 01:00 PM (CST)
Associated with  Medical Device Division

This interactive session, led by seasoned MedTech consultant Michelle Lott and Combination Product consultantSusan Neadle, will cover the practical implications of aligning FDA's requirements with the ISO standards 13485 and 14971.

This realignment aims to standardize regulatory expectations for device manufacturers.  

Please note that the starting time for the webinar is 12:00 noon Central Time (1:00 PM Eastern Time, 10:00 AM Pacific Time) While we are a non-profit organization we will have a $10 fee to help offset operational expenses. 

To get more information and register for the event either click the link or scan the QR code belowWhen you register you should receive a thank you e-mail that includes a link to the WebEx webinarIf you do not receive the e-mail or if you have questions please contact