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
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Full Circle Consulting Resources
Having high quality standards is vital to any organization but is even more essential in the pharmaceutical ...
Across all industries, documentation is a key aspect of maintaining good quality and traceability over products. ...
A 510(k) is a premarket submission made to the Food and Drug Administration (FDA) by medical device manufacturers ...
Whether looking to update an existing process or implement something brand new, process design is a critical ...
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