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Earlier this year, the Department of Health and Human Services proposed exempting 84 types of Class II devices from
One of the major purposes manufacturers incorporate AI or ML in their applications is to ease software computations
The FDA’s adverse event reporting system (FAERS) is a web-based tool that allows users to interactively search and ...
Real World Evidence (RWE) is playing an increasingly significant role in the medical device industry. The FDA has ...
When I was working on a web application as a developer, I always noticed two small issues. The identified issues ...
Medical device manufacturers know the woes of getting your product through the FDA process and onto the market. ...
Patient Safety must be at the center point of all operations in the health care industry. Whether it is the ...
Bingham Farms, MI, March 16, 2021 –E.M.M.A. International Consulting Group, Inc. (EMMA International), a global ...
Health Canada’s first Interim Order for importation and sale of COVID-19 medical devices issued on March 18, 2020, ...
Users might get frustrated with software systems in the healthcare sector due to less compact UIs or functionality ...
Almost after a year-long delay EUDAMED is finally here and has launched its first of its six modules in December ...
In today’s day and age, women’s health is more important than ever. There are several international health ...
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