Joint replacements are the #1 expenditure of Medicare. The process of approving these medical devices is flawed according to the Institute of Medicine. It is time for patients' voices to be heard as stakeholders and for public support for increased medical device industry accountability and heightened protections for patients. Post-market registry. Product warranty. Patient/consumer stakeholder equity. Rescind industry pre-emptions/entitlements. All clinical trials must report all data.
Please share what you have learned!
Twitter: @JjrkCh
Sunday, August 4, 2013
My testimony to scrap 510(k) FDA approvals of implanted medical devices 6/13/13
Labels:
510(k),
AdvaMed,
AMA,
Congress,
FDA,
hip replacement,
medical devices,
patient harm,
President Barack Obama,
product liability,
product recall,
product warranty,
surgical mesh
Dallas, TX, USA
Silver Spring, MD, USA
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