Full Circle Consulting

EMMA International can be there every step of the way for your product! From product development to helping with QMS upkeep and post-market monitoring, EMMA is here to bring your product full-circle. The expertise of the EMMA team can help you get through the biggest quality and regulatory hurdles in the life science industry with ease.

Full Service

Full Circle Consulting

When

Product Development

Regulatory Submissions

Post Market Compliance

Manufacturing and Distribution

Why

Regulatory Strategy

Quality System Development

Quality System Implementation

EMMA OnDemand

Featured Services

COVID-19

EU MDR and IVDR

MDSAP

Ready to learn more about working with us?

Full Circle Consulting Resources

510(k) Vs CE Mark

510(k) Vs CE Mark

A 510(k) is the most utilized regulatory pathway to market a medical device in the US. For a device of the same ...
What is a Notified Body?

What is a Notified Body?

If you’re considering selling your medical device in Europe, you will need a Notified Body, and you’ll need to ...

Pin It on Pinterest