Medical Devices
Device – FDA’s New QMSR – Updating 21 CFR 820 to Harmonize with ISO 13485:2016
Wednesday, November 8, 2023, 11:45 AM - 12:30 PM

On Feb. 24, 2022, the FDA published a Draft Proposed Rulemaking for the new Quality Management System Regulation (QMSR) and has pledged to make the rule final by the end of the year. Now is the time to learn the difference and similarities between the FDA unique requirements and ISO 13485:2016 requirements. This session will help you understand what you need to do to meet both sets of Quality Management Systems requirements.

Kim Trautman