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
Accelerated stability testing increases the rate of chemical degradation and physical change of a drug by using ...
In 2016 the Medical Device Single Audit Program (MDSAP) was initiated. Having a global approach to monitoring and ...
A concept similar to the FDA’s Design History Files, the EU Technical File is a collection of documents related to ...
Cosmetics are a separate category under the Food and Drug Administration (FDA) different from medical devices or ...
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