Pfizer Tries Data Digitization To Speed Spontaneous Adverse Event Reporting
Executive Summary
Combining MedWatch capabilities with electronic medical records could change the face of spontaneous adverse event reporting, providing regulatory authorities with a larger volume of more timely reports
You may also be interested in...
PDR Network's AER Tool May Add Mechanism To Reimburse Physicians For Report Follow-ups
PDR Network, in conjunction with pharmaceutical manufacturers, is looking to add a feature on its new RxEvent adverse drug event reporting application that will compensate physicians for fielding follow-up calls about reports they’ve filed.
PDR Network's AER Tool May Add Mechanism To Reimburse Physicians For Report Follow-ups
PDR Network, in conjunction with pharmaceutical manufacturers, is looking to add a feature on its new RxEvent adverse drug event reporting application that will compensate physicians for fielding follow-up calls about reports they’ve filed.
Sentinel Will Benefit From Administration's Health IT Push - FDA's Hamburg
The Obama administration's emphasis on wiring health care comes at a key time for FDA's Sentinel postmarketing medical product safety monitoring project, agency Commissioner Margaret Hamburg pointed out at a Jan. 11 public workshop in Washington, D.C