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# Device QSR Modernization/Harmonization Meeting
- URL: https://www.fdaweb.com/device-qsr-modernization-harmonization-meeting/
- Published: 2022-02-17T12:00:00.000Z
- Updated: 2026-09-14T17:33:09.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5151187

*Federal Register* notice: FDA has announced a 3/2 Device Good Manufacturing Practice Advisory Committee meeting. Panel members are scheduled to discuss and make recommendations on the current GMP requirements for medical devices in the Quality System Regulation (21 CFR part 820) and to align it more closely with an international consensus standard (International Organization for Standardization’s 13485:2016). Earlier this month, OMB completed its review of CDRH’s long-awaited proposed rule to modernize and harmonize the Quality System Regulation ([see earlier story](https://www.fdaweb.com/omb-completes-review-of-harmonized-qsr-proposed-rule/)).