1. Technical considerations for additive manufactured medical devices: guidance for industry and Food and Drug Administration staff Publication: Silver Spring, MD : Center for Biologics Evaluation and Research, December 5, 2017 Subject(s): Computer-Aided Design -- standardsDevice ApprovalManufactured Materials -- standardsMaterials Testing -- standardsPrinting, Three-Dimensional -- standardsQuality ControlComputer Security -- standardsDiagnostic ImagingModels, AnatomicProduct Labeling -- standardsReproducibility of ResultsSoftware -- standardsSterilization -- standardsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
