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
EMMA OnDemand
Quality
Quality System Development
Quality System Implementation
Post Market Compliance
ISO Standards Consulting
Operations
Product Development
Manufacturing & Distribution
Regulatory
Regulatory Strategy
Regulatory Submissions
EU MDR and IVDR
Featured Services
Clinical
Remediation
Project Management
Staff Augmentation
Mergers & Acquisitions
Ready to learn more about working with us?
Full Circle Consulting Resources
If you’re considering selling your medical device in Europe, you will need a Notified Body, and you’ll need to ...
The terms “Form 483” and “warning letter” can incite dread for those that market their medical device in the US, ...
Every medical device manufacturer in the US should expect FDA to conduct an inspection at some point, but what ...
When most people hear the term “medical device”, they think of surgical and hospital tools, like stethoscopes or ...
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