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
Cleaning validation is the first important step in reprocessing reusable medical devices. The video discusses the process for cleaning validation, considerations for doing it correctly and provides recommendations for proper...
Martell Winters and Dr. Wendy Wangsgard discuss radiation sterilization validation testing. Radiation Sterilization determines appropriate radiation sterilization doses for products which require a sterile label claim. It incorporates bioburden testing,...
Ethylene Oxide sterilization is well known in the industry and is accepted as a sterilant by the FDA. It is one of the most popular ways of sterilizing medical devices....
President/CEO Jeffery Nelson talks about Nelson Laboratories testing capabilities for medical device manufacturers at MD&M West 2010. He also discusses the companies history, uniqueness, and dedicated scientists. Nelson Laboratories is...
