Collaboration with EMCI is easy.

Whether you simply need an existing tool or device redesigned or upgraded, or you have a new idea that needs to be developed, EMCI has the experience to get the job done. Because of our many years of experience and our impeccable quality standards, we can handle every phase of your product's design, development, testing, regulatory approval, patent, manufacturing, and after-sales service. Your medical expertise is put to work during the testing and trials phase, and your critical input will ensure that the product works exactly the way you want.

EMCI handles engineering.

Our engineering department can handle both design engineering and manufacturing engineering. Prototypes are designed and built in-house, so we have full control over the output. As a medical professional, you can participate as much or as little as you like during the prototyping phase. We find that most doctors and surgeons want to have hands-on participation.

EMCI handles regulatory approvals.

The most important, and frequently the most difficult phase of new product development is regulatory compliance and approval. EMCI's experienced quality department can navigate the regulatory system for you and make sure everything is done according to FDA and ISO standards, as well as any other regulatory bodies that apply to your device (e.g. UL, CE, MET, etc.)

We walk you through, every step of the way.

Even if your concept only exists in your head, we can start the process with simple dialogue. You don't need to be an expert in engineering or manufacturing, or even an expert at drawing or sketching. We make it simple for medical professionals to have devices with their name on them... we are collaboration experts. Click the link below to start a confidential, no-obligation dialogue today!

collaborate@epicmedical.net