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ISO 26262 - Effectively Managing the Safety Development Cycle with a Software System Lifecycle Management Platform
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ISO 26262-konform mit Application Lifecycle Management
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Making Agile Work in Highly Regulated Environments
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Manage Complexity in Shorter Release Cycles: Software Product Lines (SPL) and Variant Management
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Managing the Exchange of Software and System Requirements: Collaborating Across Boundaries with the Requirements Interchange Format (ReqIF) - Featuring Integrity & AgoSense
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Medizinische Software standardkonform entwickeln
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Military Embedded Systems E-Cast, Sponsored by MKS: Modern Practices for Effective Development of DO-178B/C Compliant Software
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Modern Practices for Effective Development of DO-178B/C Compliant Software
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Navigating International Standards and Regulations for Medical Devices – A Presentation on ISO standards, the FDA and the European Medical Device Directive
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Predicting Product Release Readiness with Integrity
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Reclassification of MDDS as Class 1 Devices: Implementing a Compliant Quality Management System
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Reusing Requirements, Tests Cases and Components Across Product Lines - A Successful Approach for Improving Auditability, Quality and Time to Market
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Revealing the Secret of Requirements Reuse
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SAE's Automotive Engineering International and MKS Present: Functional Safety and ISO 26262 - Essential Tools and Strategies for Compliance (Featuring Doris Wild, Expert for Functional Safety, TÜV SÜD Automotive)
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Shorten Application Delivery Time with Requirements-Based Testing (RBT)
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Solving the Engineering Change & Complexity Challenge
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Solving the Quality and Compliance Challenge for Medical Devices with Integrity
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Stickyminds Webinar, Featuring MKS - Metrics that Matter to the Agile Organization: Measuring for Progress and Quality
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Stickyminds Webinar, Sponsored by MKS and featuring OVUM: Software Development and the Product Lifecycle - When Worlds Collide
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The Opportunities and Challenges of Risk Management Compliance in Medical Device Engineering
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