The contract research organization will launch an expanded ISO 18562 gas pathway testing program and ISO 10993-18 particulate ...

FDA uses a range of biocompatibility test data to evaluate medical devices before clearing or approving them for marketing. The growing use of FDA-recognized consensus standards facilitates this ...

Medical device manufacturers use cytotoxicity testing to help prove that devices that come into contact with the human body are biocompatible. Testing results are critical for gaining market access, ...

Stability studies measure how medical devices respond to environmental stresses such as temperature, humidity, light, and ...

PITTSBURGH, PA, UNITED STATES, January 5, 2026 /EINPresswire.com/ — Barbara F. of Aurora, CO is the creator of Magnifier Plus ...

Medical device design and development has evolved over the years, notably influenced by market demands and regulatory requirements. Traditional design practices, beginning with a reliance on generic ...