Medical Device Reports To FDA Rose 77% In 2006
This article was originally published in The Gray Sheet
Executive Summary
The number of adverse events reported to FDA under the Medical Device Reporting (MDR) program rose last year to an all-time high, and agency staffers predict the trend will continue through 2007
You may also be interested in...
In Search Of Missing Adverse Events, U.K. Looks To Expand Online Reporting
The United Kingdom's device regulators are trying to reverse a trend of under-reporting of medical device adverse events by health care practitioners
In Search Of Missing Adverse Events, U.K. Looks To Expand Online Reporting
The United Kingdom's device regulators are trying to reverse a trend of under-reporting of medical device adverse events by health care practitioners
CDRH Considers Internet Forum To Aid Device Safety Surveillance
FDA's device center is assessing whether an online forum for physicians can help with its postmarket surveillance challenges