According to the ISO standard 10993, a medical device should be biocompatible i.e. not induce any adverse effects when it comes in contact with the patient. The standard provides a […]

Medical Device biocompatibility, once considered just a "box-checking" activity, continues to become more complex. This was the focus of a talk at the 2012 American College of Toxicology Annual Meeting […]

Increasingly, device makers are discovering what pharmaceutical companies have known for many years – that using CROs to support regulatory testing can speed up development efforts and, ultimately, save money. The […]