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 last blog post reviewed how 3D printed medical devices present unique challenges from a biocompatibility assessment perspective due to their highly customized material properties. Additives to raw materials used in 3D printing are required to enhance workability. For 3D...
The use of three-dimensional (3D) printing techniques to address challenging fabrication problems has become mainstream over the past decade. While this rich resource has extended fabrication of personalized medical devices to the limit of our imagination, the myriad materials and...
Thor Rollins, consulting manager, and Audrey Turley, research scientist, have been invited to speak at the joint conference of the Association of Analytical Communities Southern California Section (AOAC SCS) and Food and Drug Agency (FDA) 2016 Spring Conference. Rollins and...
When dealing with orthopedic medical devices, even small changes in the manufacturing process or device materials can impact patient safety. With these changes comes the risk of introducing new compounds that may leave residue on the device or leach harmful...
Scientists at Nelson Laboratories recently returned from presenting new in vitro research at the 2015 Society of Toxicology (SOT) annual meeting with news that the future of in vitro testing of medical devices in the United States looks bright, and...
