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

Third-Party Review of 510(k)s

Third-Party Review of 510(k)s

FDA is not the only organization that can review 510(k) submissions. Under the Third Party (“3P”) Review Program, ...
Your 2019 Wish List!

Your 2019 Wish List!

We witnessed several changes in the medical device industry in the year 2018. The impact of some changes was ...

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