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
Register HERE for the three-day live webinar series “How to Develop a Risk-Based Safety Evaluation per New US FDA Guidance” presented by Nelson Laboratories’ experts: Thor Rollins, Sarah Campbell, and Audrey Turley. This three-day webinar will incorporate the new US FDA...
“The radiation sterilization AAMI committee is offering a great opportunity for manufacturers to communicate their real-life needs – and we want to hear from you! We are trying to gather data on the use of the VDmax method in the...
Incorporating Biocompatibility, Chemistry, and Toxicology into your Biological Risk Evaluation In the past, biocompatibility consisted of determining the contact of your medical device, looking at the Table A.1 in ISO 10993-1 and running the test prescribed. This approach put too...
We are excited to share the news that our Nelson Labs facility in Itasca, IL significantly expanded lab operations and testing capabilities to better serve our customer needs. Lab customers will benefit from state-of-the-art facility and equipment upgrades to the...
It was recently announced that Martell Winters, B.S., RM/SM(NRCM) was appointed and approved as convenor for a three-year term of a new ISO working group, WG16, on vaporized hydrogen peroxide sterilization. The new working group is tasked with developing a new...
