When the concept designs have been narrowed down to a handful of possibilities, the concept phase ends and the feasibility phase begins. During the feasibility phase, development engineers begin working on the design input requirements (DIR) necessary for the final product design. The development team also works on intellectual property documents and assists quality engineers with drafting the design Failure Mode & Effects Analysis (FMEA) document(s). A secure document control solution for organizing, storing, routing, updating, approving, releasing, and quickly locating design documents, as well as the intellectual property, FMEA, and other documents greatly facilitates the cross-functional team's efforts.
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Controlled Documents Managed in the Feasibility Phase
Collaboration Workflows in the Feasibility Phase
To have a comprehensive view of how MasterControl supports medical device companies in feasibility phase, feel free to contact MasterControl representative today.