COVID-19 Consulting
The COVID-19 pandemic has introduced unprecedented challenges to the medical device and life-sciences industry. From PPE shortages, remote audits, delays in regulatory processes, and much more.
EMMA International has stayed on top of the ever changing quality and regulatory landscape amidst the global public health emergency and has compiled the following resources to keep the life-science industry informated, to ensure life-saving products get to market, and stay on the market.
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COVID-19 Resources
Since its inception, EMMA International has been dedicated to providing consulting services to help ensure ...
After over 3 years, the COVID-19 Public Health Emergency (PHE) will end on May 11, 2023, the Biden Administration ...
It is no surprise to anyone in the medical device industry that the transition from EU MDD to EU MDR has seen ...
A ‘CS’ was to be a ‘Common Specification,’ intended to satisfy the EU MDR requirements. If you were working to ...