You can do better than just meeting compliance requirements. Get detailed advice from engineering and product development experts on how to build a quality foundation that allows you to innovate faster, provide full traceability throughout the device lifecycle, and create True Quality medical devices with less risk.
Experts speaking about Go: What You Need to Know to Get New Devices to Market with Less Risk
Talks related to Go: What You Need to Know to Get New Devices to Market with Less Risk
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4 Quality System Musts for Medtech Startups to Get Safer Products to Market Faster
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An Inside Look at Changes to the New ISO 14971:2019 from a Member of the Standard’s Working Group
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When to “Flip the Switch”- Balancing Late Feasibility and Early Design Controls
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Design Considerations to Maximize Medical Device Cloud Connectivity
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Game Changing Product Definition Tactics
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Medical Device Project Pitfalls and How to Avoid Them
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Why Design Validation is More Than Testing: How do we validate our validation?
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How User Experience Design and Human Factors Engineering can Accelerate Product Development
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Best Practices for Preparing and Conducting Pre-Submission Meetings
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