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
When reporting an Adverse Event to the Food and Drug Administration (FDA) the best method is to utilize the FDA ...
A device can be registered for the De Novo pathway if there is evidence of the safety and effectiveness of the ...
There are three types of 510K, Premarket Notifications, which can be submitted to the Food and Drug Administration ...
Many marketed products are classified as medical devices and you would not even know it. Medical devices range ...
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