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Agenda
Reg Review
ICR
Information Collection List
IC Title
Status
Responses
Hours
Dollars
Document Type
Form No.
Form Name
Animal Drug Adverse Event Information Collection Activities
Modified
124444
172276
0
Form and Instruction
FDA 1932
VETERINARY ADVERSE DRUG REACTION, LACK OF EFFECTIVENESS, PRODUCT DEFECT REPORT
Form and Instruction
FDA 1932a
VETERINARY ADVERSE DRUG REACTION, LACK OF EFFECTIVENESS, OR PRODUCT DEFECT REPORT (voluntary reporting)
Form and Instruction
FDA 2301
TRANSMITTAL OF PERIODIC REPORTS AND PROMOTIONAL MATERIAL FOR NEW ANIMAL DRUGS
Drug experience reports; advertisements and promotional labeling; distributor statements
Removed
0
0
0
Form and Instruction
2301
Transmittal of Periodic Reports and Promotional Material
Other-Screenshots - Proposed Electronic Submitter System
Medicated feed reports
Removed
0
0
0
One time recordkeeping resulting from implementation of new requirements (New SOPs and training)
Removed
0
0
0
Recordkeeping requirements under 510.301 and 514.80
Modified
124444
1742136
0
Request for waiver from electronic reporting requirement
Removed
0
0
0
Voluntary adverse event reporting
Removed
0
0
0
Form and Instruction
1932a
Veterinary Adverse Drug Reaction, Lack of Effectiveness
Total burden requested under this ICR:
248888
1914412
0
To view an IC, click on IC Title