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
When
Product Development
Regulatory Submissions
Post Market Compliance
Manufacturing and Distribution
Why
Regulatory Strategy
Quality System Development
Quality System Implementation
EMMA OnDemand
Featured Services
COVID-19
EU MDR and IVDR
MDSAP
Ready to learn more about working with us?
Full Circle Consulting Resources
Submitting a 510k for a medical device can be a long and confusing process. When a 510k is submitted the device ...
The COVID-19 pandemic has changed the world by disrupting global supply chains and impacting human health. This ...
A Certificate of Analysis, CoA, is a document, usually issued by an organization’s quality department, that ...
A deviation is any unwanted event that differs from the approved processes, procedures, instructions, ...
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