In a society that thrives on innovation, companies are constantly attempting to come up with new ideas to improve patient care and treat a variety of medical issues. However, while this might be an admirable endeavor, studies suggest that it might be necessary to revise the regulations concerning the manner in which each product is approved for use. One area of concern in the study relates to the regulation that allows a company to seek approval by showing that a device is substantially equivalent to products that are already being used.
Even with clinical data indicating the safety of products such as surgical mesh and hip implants, thousands of individuals have experienced severe harm due to flaws within these devices. Patients who have a device implanted within their bodies should be made aware of any potential risks associated with a product. However, without changes to testing procedures, some of these risks may continue to go unnoticed until disaster strikes.
Those who suffer severe injuries due to defective medical devices may wish to exercise their rights to pursue restitution, but they might need assistance in the process. When facing a similar situation, a person could choose to speak with an attorney for guidance on how best to proceed. An attorney in Tennessee can assist a client in pursuing the full amount of compensation available through a claim against the party or parties deemed liable.