Brooks asks if the orthopaedic companies are above the law?
it’s now become apparent that for those of us in the US, and seemingly the rest of the world, for …
Tag Archives: Washington D.C.
FDA surveillance operation draws criticism from lawmakers | Reuters
FDA surveillance operation draws criticism from lawmakers | Reuters. FDA surveillance operation draws criticism from lawmakers WASHINGTON | Sun Jul …
J&J-Led Vaginal Mesh Group Says FDA Should Require More Studies
J&J-Led Vaginal Mesh Group Says FDA Should Require More Studies September 08, 2011, 4:42 PM EDT Source: Bloomberg By Alex …
US Congress Women Rosa L. DeLauro Takes FDA To Task Over Comments re IOM Report
For Immediate Release Friday, July 29, 2011 Contact: Kaelan Richards 202-225-3661 DELAURO TO FDA: 510(k) MEDICAL DEVICE APPROVAL PROCESS UNSAFE, …
510(k) approval process is too big to fail no matter how flawed it may be
7.29.11 | Arundhati Parmar Source: MedCityNews 510(k) approval process is too big to fail no matter how flawed it may …
FDA 510K Process – Another Issue – Risky pelvic mesh highlights worries about FDA process
Risky pelvic mesh highlights worries about FDA process Untested medical devices found to erode patients’ insides Source: MSNBC.com By Rita Rubin; …
CDC Links Obesity, Arthritis, and Lack of Exercise
CDC Links Obesity, Arthritis, and Lack of Exercise Study Shows Obese Adults Who Have Arthritis Are More Likely to Skip …
Corin Cormet FDA Approval – At Least the FDA Panel included Metal Ion Serum Levels
Orthopaedic and Rehabilitation Devices Panel – February 22, 2007 The Orthopaedic and Rehabilitation Devices Panel (the Panel) met on Thursday, …
