Premarket Approval (PMA) Process - Medical Device Safety
The Premarket Approval (PMA) process is the FDA's most stringent for approving medical devices. PMAs are rare & costly so manufacturers typically avoid it.| Drugwatch.com
The Premarket Approval (PMA) process is the FDA's most stringent for approving medical devices. PMAs are rare & costly so manufacturers typically avoid it.| Drugwatch.com
A health care desert has emerged in Delaware County. There are currently only two hospitals, Riddle and Mercy Fitzgerald, operating […]| Broad + Liberty
Viagra is the “little blue pill” capable of treating erectile dysfunction (ED), but recent studies have linked the drug to an increased risk for melanoma.| Drugwatch.com
The FDA 510(k) clearance process allows medical devices to enter the U.S. market with no clinical trial requirement and no evidence that they are safe.| Drugwatch.com
The U.S. Food & Drug Administration regulates drugs and medical devices. It also collects reports on adverse events from these products.| Drugwatch.com
