Archives for December 2014
By: Jeff S. Gibson, Attorney
The pharmaceutical and medical device industry seems to be on an endless search for the next advancement to improve patient care and quality of life. Whether existing designs are significantly altered by the addition of new materials or new products are created, the FDA continues its oversight of these devices and provides the final approval to allow these products on the market.
As medical device manufacturers rush to market products designed to help patients experience a better quality of life, incomplete or deficient research and reports required to obtain FDA approval can put patients at risk.