PRA IC List
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Agenda
Reg Review
ICR
Information Collection List
IC Title
Status
Responses
Hours
Dollars
Document Type
Form No.
Form Name
Adverse Experience Reporting for Licensed Biological Products 21 CFR 600
Migrated
645
8329
0
Form
FDA-3500
Form
FDA-3500A
Total burden requested under this ICR:
645
8329
0
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The .gov means it's official.
The site is secure.
