The new cleanroom at our global headquarters in Salt Lake City, Utah, was designed for today's rigorous contamination control expectations, driven by EU GMP Annex 1. Learn More
The European standard, EN 13795, addresses the barrier properties, cleanliness, and strength of surgical drapes, gowns, and clean air suits used to protect patients from secondary infections in the surgical suite. The standard was approved in 2011, updated in 2013,...
During the annual Society of Toxicology (SOT) meeting in Baltimore, Maryland, Michelle Lee and Audrey Turley from Nelson Laboratories were two of eleven authors awarded Best Overall Abstract for “Round Robin Study to Evaluate the Reconstructed Human Epidermis (RHE) Model...
At Nelson Laboratories, our values hinge on quality, service, and expertise. Our quality systems and world-class facilities are part of what elevates us in the MedTech industry. We recently completed a two-year renovation to our state-of-the-art ISO Class 5 cleanroom....
MedTech innovation leaders gathered at the University of Texas in San Antonio to share their expertise with up-and-coming biomed talent. The Health Cell, a life sciences professional development and advocacy organization, created a pilot workshop series Developing and Clinically Introducing...
Device manufacturers that incorporate particulate testing into their product-development plans early are better equipped to navigate the regulatory clearance process and potentially reduce time to market. Particulate testing of cardiovascular medical devices is an important and valuable step on the...
