by canyonlabsstg | Dec 2, 2025 | Blog
For pharmaceutical and medical device manufacturers, ensuring that a product is sterile is one of the most critical steps in protecting patient health and meeting regulatory requirements. Sterility assurance testing provides the data and validation needed to...
by canyonlabsstg | Oct 21, 2025 | Blog
When political gridlock hits Washington, the ripple often reaches all the way to the manufacturing floor. For medical device companies, a government shutdown is more than a headline. It can directly affect timelines, reviews, and regulatory confidence. At Canyon Labs,...
by canyonlabsstg | Oct 15, 2025 | Blog
Advancing Patient Safety with Expert Toxicological Risk Assessments At Canyon Labs, we know that patient safety depends on more than just product performance—it requires a deep understanding of potential chemical risks intrinsic to materials of construction,...
by canyonlabsstg | Sep 4, 2025 | Blog
What is Irritation Testing? A key component of biocompatibility testing is irritation testing, which directly assesses the potential of a material or product to cause localized irritation upon contact with sensitive tissues. Irritation testing is performed in vivo,...
by canyonlabsstg | Aug 19, 2025 | Blog
Introduction Sensitization testing is designed to rule out the potential for allergic reactions that can result from exposure to a medical device, material, or pharmaceutical product. These delayed hypersensitivity reactions can occur when the body’s immune system...
by canyonlabsstg | Jul 29, 2025 | Blog
Executive Summary In today’s dynamic regulatory and supply chain landscape, more medical device and pharmaceutical manufacturers are exploring changes to their sterilization methods. These shifts are often driven by growing environmental concerns, evolving regulatory...
