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


Product Development

Regulatory Submissions

Post Market Compliance

Manufacturing and Distribution


Regulatory Strategy

Quality System Development

Quality System Implementation

EMMA OnDemand

Featured Services




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Full Circle Consulting Resources

Regulatory 101 for Medical Device Start Ups

Regulatory 101 for Medical Device Start Ups

In this webinar hosted from EMMA International's Lead Quality Engineer, Nikita Angane, she will go over the different FDA Centers, as well as the pathways to market, what a RTA (Refuse to Accept) is, and also reviewing labeling, registration, and device listings.
FDA Export Certificates

FDA Export Certificates

Manufacturers that export FDA-regulated products such as drugs and medical devices from the US are oftentimes ...

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