FDAFrom FDA - Page 6FDA Final Guidance: Form and Content of the Unique Device Identifier (UDI)Enforcement Policy Regarding Use of National Health Related Item Code and National Drug Code Numbers on Device Labels and PackagesExpedite Med Device Approval with FDA’s New ProgramHow FDA Food Supply Data Supports COVID-19 Vaccine DistributionAdvanced Automation Tools May Be Just the Panacea Our Industry NeedsFDA Dec. Meeting: Drug Supply Chain Security Act Pilot Project ProgramCORE Outbreak Investigation Table IssuedFDA Guidance on Voluntary Disclosure of SesameVoluntary Pilot Program for Third-Party Food Safety StandardsFDA Establishes the U.S. Agent Voluntary Identification System for Food FacilitiesFDA Provides Additional Flexibility Regarding Nutrition and Supplement Facts LabelsFDA Guidance: Expiration Dating of Unit-Dose Repackaged Solid Oral Dosage Form Drug ProductsPrevious PagePage 6 of 15Next Page