Form 3500A MEDWATCH

Adverse Experience Reporting for Licensed Biological Product; and General Records

FORM FDA 3500A MEDWATCH

600.80(i)

OMB: 0910-0308

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File Typeapplication/pdf
File TitleFORM FDA 3500A
SubjectMEDWATCH - for Mandatory Reporting
AuthorPSC Publishing Services
File Modified2014-11-03
File Created2013-12-13

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