Resource Center
Find the latest content and resources from our team of experts to keep you in the know for all things quality and regulatory in the life science industry.
Sort by topic
Sort by resource type
One of the most common techniques to prevent contamination of products and reduce quality impacts in the ...
Having high quality standards is vital to any organization but is even more essential in the pharmaceutical ...
Across all industries, documentation is a key aspect of maintaining good quality and traceability over products. ...
A 510(k) is a premarket submission made to the Food and Drug Administration (FDA) by medical device manufacturers ...
Whether looking to update an existing process or implement something brand new, process design is a critical ...
Since its inception, EMMA International has been dedicated to providing consulting services to help ensure ...
Accurate and precise measurements are vital in the pharmaceutical, medical device, and other FDA regulated ...
Many controls are well-designed and put in place to help drive and maintain the quality of the sterile drugs ...
How does a medical device manufacturer make sure that they prevent garbage from coming into their factory, and ...
The European Commission has implemented a proposal to extend the transitional period to certify medical devices ...
After over 3 years, the COVID-19 Public Health Emergency (PHE) will end on May 11, 2023, the Biden Administration ...
All right, you have just gotten all of your paperwork together, submitted the right forms to the right people, set ...
Ready to learn more about working with us?
