This interactive session, led by seasoned MedTech consultant Michelle Lott and Combination Product consultant Susan 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 below. When you register you should receive a thank you e-mail that includes a link to the WebEx webinar. If you do not receive the e-mail or if you have questions please contact bobshanks52@hotmail.com.