February 2012 www.citizen.org Regulation of medical devices—a $350 billion industry that includes such products as heart and brain stents, artificial hips and implantable defibrillators—is at a crossroads. With a major reauthorization bill up for debate, members of Congress already have introduced 14 bills that aim to accelerate devices’ path to the market, often by weakening measures intended to ensure patient safety. Read more
Substantially Unsafe – Medical Devices Pose Great Threat to Patients; safeguards Must be Strengthened, Not Weakened
This entry was posted in Newsroom, Patient Safety Activism and tagged FDA, Food and Drug Administration, health care reform, Medical Device Amendments of 1976, Medical Device User Fee Act (MDUFA), medical devices. Bookmark the permalink.
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