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

Thursday, October 20, 2011

Mercury Fillings are a Failed Implanted Medical Device FiDA

(link) Cautionary YouTube video about mercury toxicity and dental amalgam

FDA Town Hall meetings in Irving, TX  3/10/11 and San Francisco 9/22/11 were attended by speakers on this topic.

No comments:

Post a Comment