FiDA         Failed Implant Device Alliance

Showing posts with label Katie Thomas. Show all posts
Showing posts with label Katie Thomas. Show all posts
Thursday, March 3, 2016

FDA Commissioner Dr. Califf: The Fox is in the Henhouse!

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F.D.A. Asks If Faulty Blood Monitor Tainted Xarelto Approval By KATIE THOMAS   FEB. 22, 2016 The Food and Drug Administration is inves...
Wednesday, March 2, 2016

Any COI? Dr. Robert Califf: FDA Commissioner and former Duke University researcher.

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Document Claims Drug Makers Deceived a Top Medical Journal By KATIE THOMAS MARCH 1, 2016 It is a startling accusation, buried in a foo...
Wednesday, May 27, 2015

F.B.I. Investigates: Are Medical Device Adverse Events Reported?

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F.B.I. Investigates Whether Harm From Surgical Power Tool Was Ignored By DENISE GRADY and KATIE THOMAS  MAY 27, 2015 The Federal Bur...
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Sunday, September 9, 2012

Patient Last To Know About Implant Danger

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September 7, 2012  The New York Times Unpredictable Danger Looms Close to the Heart By KATIE THOMAS Monsters atta...
Wednesday, June 6, 2012

Smarmy corporate action: surgical mesh

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http://www.nytimes.com/2012/06/06/business/johnson-johnson-unit-will-stop-selling-urinary-implants.html?emc=tnt&tntemail1=y June 5...
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Joleen Chambers
Goals: implant product warranty, unique device identifier UDI, independent patient outcome registry, legal patient protections for continued care
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