A Systems Approach for efficient and compliant design and development of Medical Devices
What are you trying to build? How will you define “success”? How will the product be used? Do you know how to test the product? How will the architecture be organized? What do you need for regulatory clearance or approval?
This whitepaper examines an approach to developing requirements in a manner that provides the critical framework needed to develop your product without overburdening the effort with endless paperwork and testing.
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