Arrotek’s whitepaper outlines three essential phases for medical device manufacturing success: Design for Manufacture (DFM), Design Transfer, and Continuous Improvement. DFM focuses on optimizing product designs for efficient, cost-effective production while meeting quality standards. Design Transfer ensures seamless regulatory-compliant transition from design to manufacturing. Continuous Improvement addresses ongoing enhancements to processes and product quality, navigating the complexities of medical device manufacturing. Partnering with Arrotek’s Contract Design and Manufacturing Organization (CDMO) supports manufacturers in achieving compliance, efficiency, and innovation throughout the device lifecycle.

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