“Challenges & Solutions for Reusable Medical Devices Requiring Reprocessing”
There’s been an important development in the 2016 FDA science priorities that involves taking a stronger look at the reprocessing cycle and the impact on reusable medical devices. The regulations aim to enhance technologies associated with reprocessing as well as the related design of the medical devices. And as reprocessing gets more focus and attention, this development will naturally lead to a closer examination of the device design characteristics and relation to life-cycle and fit-for-use properties. Read more ›
