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Product Overview - Quality Management - Software Engineering ISO 9001 Quality Management Development Tools ISO/IEC 27001:2013 - Security Requirements ISO/IEC 27001:2017 - Software Security Requirements ISO/IEC 27002:2013 Security Code of Practice ISO/IEC 27018:2014 - Security Management Software Security ISO/IEC 27001, ISO/IEC 27002, ISO/IEC 27018 For Medical Devices, Checklists, Guides for FDA Related Software ISO 13485:2016 - Medical Devices, Software Requirements ISO 9003 - ISO/IEC 90003
ISO 9004:2009 for a Successful Quality Management Approach IEC 62304:2015 Medical Device Software - Life Cycle Process ISO/TS 16949:2009 Documentation Model, Requirements Checklist FDA Software Validation System and Software Engineering, Tools, Guides, Checklists Templates for Software Configuration Mgmt. and Maintenance Templates for System - Software - Document Management Guide to Software Eng. Standards Development and Maintenance ISO/IEC 15288:2008 Compliance ISO/IEC 20000-1:2011 Information Technology FDA 21 CFR Compliance Requirements ISO/IEC/IEEE 42010:2011 - Architecture Description Checklist FDA Off-the-Shelf Software in Medical Devices Quality Software Standard Checklist Kit ANSI/UL 1998:2004 Compliance Guide Reference

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