Some transvaginal mesh complications and safety risks can be serious. Learn about potential dangers, FDA warnings and legal actions.| Drugwatch.com
Consumers are filing lawsuits against prescription drug and medical device companies after facing serious injuries. Find out if you qualify for a lawsuit.| Drugwatch.com
Learn about common knee implant complications, defective devices, recalls and lawsuits.| Drugwatch.com
Learn why hip replacements fail, common complications like loosening or infection and how to recognize warning signs early.| Drugwatch.com
More than 13,000 drugs and medical devices have been recalled in the past few years for reasons ranging from defective packaging to fatal side effects.| 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
The FDA approval process can be long and tedious however there are ways to fast-track approving a new drug or device through different FDA applications.| Drugwatch.com
A division of the FDA oversees a broad range of medical devices, from scalpels to stethoscopes and from artificial hips to transvaginal mesh.| Drugwatch.com
Learn about the FDA's clinical trial stages and phases used to determine new ways to prevent, screen for, diagnose and treat diseases or conditions.| Drugwatch.com
Big Pharma consists of powerful drug manufacturers that are often accused of unethical marketing practices and promoting dangerous medicines.| Drugwatch.com