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
Project Management
Staff Augmentation
Ready to learn more about working with us?
Full Circle Consulting Resources
Engaging in medical device product development requires establishing and documenting design controls. The FDA ...
The new EU MDR 2017/745 is complex, to say the least. Depending on a company’s relationship to the medical device ...
When making a new product, whether that product is a drug, a medical device, or a combination product, ...
When an error occurs, corrective and preventative actions are developed to help strengthen the quality ...
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