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

Saturday, August 27, 2011

Please sign Petition to Congress and President Obama

Sign and share with your friends/family! Thank you!  (revised link)

When I speak at the FDA/CDRH Town Hall meeting in San Francisco on 9/22/11 I will be speaking for all of you.

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