Last updated on JANUARY 10, 2014
Applies to:Adverse Event Reporting System - Version 4.6.0 to 4.6.2 [Release 4.6.0]
Information in this document applies to any platform.
***Checked for relevance on 10-JAN-2014***
The Medwatch form generated from AERS displays "FDA Facsimile Approval 06/23/98 (Oracle)" whereas the Medwatch form for Mandatory reporting on the FDA website displays "Form Approved:OMB No. 09 10-029 1, Expires 12/31/11".
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