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.
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Full Circle Consulting Resources
The purpose of this webinar is to discuss the FDA’s voluntary medical device manufacturing and product quality pilot program, CMMI Institute’s role in it and how manufacturers will benefit from this program.
The FDA’s 510(k) process for medical devices is doing a lot of rounds in the news lately. This includes the FDA ...
![A Brief Analysis of Medical Device Quality System Enforcement Actions [2015 -2017]](https://emmainternational.com/wp-content/uploads/2018/11/AnalysisOfMedicalDevice_Blog-gap.png)
Every year FDA releases an annual report for Quality system inspections and enforcement action data for the ...
The revision of the Quality System Regulation [QSR] (21CFR 820) which was a priority set in FDA’s Spring unified ...
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