Why It’s Important to Partner with an Expert for Medical Device Design & Development

Design and development (D&D) of a medical device is the most crucial phase of the product’s route to market for its success.

A loosely defined and designed product cannot comply with regulatory needs and it will fail to deliver the user-defined functionality and benefits.

Many designers and manufacturers have different processes to achieve the same thing. Partnering with Mi3 on the journey to design & develop your device, or assist in this process will ensure that every consideration is made from Regulatory Strategy and D&D planning to meeting end-user needs compliantly, cost-effectively and ensuring patient safety.

We discuss seven key steps in the D&D process and the critical outputs an experienced contract manufacturing partner can bring to the process.

To read more, please download this free white paper.

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