Shaping The Regulatory Landscape For A New Generation Of Devices
Shaping the regulatory landscape for a new generation of devices
New digital elements in medical devices are shaping a modern approach to patient care. These novel elements provide benefits in the form of new market participants, who have in turn brought innovation and new manufacturing processes. Ahead of his participation in the Software Design for Medical Devices Global Forum, we spoke to Pat Baird, Regulatory Head of Global Software Standards, Philips about the impact that the latest software developments are having on regulating a new generation of medical devices.
Please note: That all fields marked with an asterisk (*) are required.
*Processing your payment may take a moment. Please click submit payment only once, and do not refresh this page. Doing so may result in your credit card being charged more than once.