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.
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Twitter: @JjrkCh

Monday, August 22, 2011

My brother, Steven Baker, a personal story . . .YouTube video

8 minute video- includes action items for assuring that implanted medical device innovation is
 balanced with adequate protections for patients.

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