With the ability to 3D print anything from a house to a bionic arm it’s...
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.