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
Download this whitepaper to examine the various ways in which chemical characterization can augment and refine the biocompatibility testing process. Using analytical chemistry and data from the compound libraries to assess the finished device can yield more specific data about...
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...
Several noteworthy changes are anticipated in a new FDA guidance document on biological evaluation and biocompatibility testing of medical devices due out sometime this year. Read the Full Story in MD&DI Online
