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
The UDI Rule requires a device to bear a UDI on its label and packages. Special labeling requirements apply to ...
Last week, the FDA finalized guidance for medical device establishment inspections, which satisfies a requirement ...
FDA released a guidance document on Monday in the form of a question and answer format to help the industry ...
The COVID-19 pandemic has forced some of the most drastic loosening of regulatory requirements the FDA has ever ...
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