FDA readies new data systems for drug safety

The Food and Drug Administration will expand its tracking of drug safety once the drugs enter the marketplace, according to a new report.

FDA plans electronic filing for some safety reports

Proposed rules announced today would require that all mandatory post market reporting of adverse effects for drugs and medical devices be filed electronically, either through a gateway, a Web portal under development, or on disk or tape.

FDA puts Web site search in a nutshell

The Food and Drug Administration used Google Search Appliance to compile an online list of hundreds of recalled peanut products.