Content by Oriel STAT A MATRIX
More Stringent FDA Review Processes for Medical Devices on the HorizonThe FDA prepares to review and revise the 510(k) process.
Mon, 03/08/2010 - 15:09
After years of focusing on the pharmaceutical industry and establishing better controls for reviewing the safety and efficacy of pharmaceutical products prior to approval, the Food and Drug Administration (FDA) is now directing its attention to the…
