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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Tuesday, June 7, 2016

#Cinderblocks3 presentation: 20 slides, 20 seconds each on PREVENTABLE harm from implanted medical devices

NO AUDIO, the slides advance automatically.   FiDA highlight

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