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The unique device identifier (UDI) might not be the most exciting U.S. FDA enforcement mandate for most of regulated industry, but the FDA’s Keisha Thomas indicated that compliance is less than adequate in the agency’s view.
FDAnews Announces FDA Drug GMP Facility Inspections During the Pandemic Webinar March 10, 2021 PRWeb FacebookTwitterEmail FALLS CHURCH, Va. (PRWEB) February 24, 2021 FDA Drug GMP Facility Inspections During the Pandemic An FDAnews Webinar Has one’s inspection timeline been thrown for a loop because of COVID-19? How exactly will sites move forward with the FDA? The FDA restarted inspections last summer under a new guidance and during this webinar FDA inspections expert Kalah Auchincloss will share how assessments are proceeding and what criteria the FDA is using to determine which sites are...