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
Project Management
Quality
Quality System Development
Quality System Implementation
Post Market Compliance
ISO Standards Consulting
Operations
Product Development
Manufacturing & Distribution
Government Contracting
Supply Chain
Regulatory
Regulatory Strategy
Regulatory Submissions
EU MDR and IVDR
Featured Services
Clinical
Mergers & Acquisitions
Remediation
Engineering
Staff Augmentation
Ready to learn more about working with us?
Full Circle Consulting Resources
The regulatory landscape of women's health in the United States has evolved significantly over the past century, ...
Packaging validation is more than just a regulatory requirement—it's a fundamental aspect of medical device ...
For medical device and pharmaceutical companies, quality is a cornerstone of success. It ensures regulatory ...
Submitting a 510(k) application is a crucial step in getting a medical device cleared by the FDA for marketing in ...
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