Information Collection

Animal Drug Adverse Event Information Collection Activities

IC 37624 under ICR 202512-0910-008 · OMB 0910-0284.

Information Collection (IC) Details

View Information Collection (IC)

Animal Drug Adverse Event Information Collection Activities
 
No Modified
 
Mandatory
 
21 CFR 514.80 21 CFR 510.301

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Form and Instruction FDA 1932 VETERINARY ADVERSE DRUG REACTION, LACK OF EFFECTIVENESS, PRODUCT DEFECT REPORT FDA-1932_Stat_Sec_Ext_Exp 08_2026.pdf Yes Yes Fillable Fileable
Form and Instruction FDA 2301 Transmittal of Periodic Reports and Promotional Material for New Animal Drugs FDA-2301_Stat_Sec_Ext_Exp 08_2026.pdf Yes Yes Fillable Fileable
Form and Instruction FDA 1932a VETERINARY ADVERSE DRUG REACTION, LACK OF EFFECTIVENESS, PRODUCT DEFECT REPORT (VOLUNTARY) FDA-1932a_Stat_ext_sec_Exp 08_2026.pdf Yes Yes Fillable Fileable

Health Consumer Health and Safety

 

476 0
   
Private Sector Businesses or other for-profits
 
   100 %

  Requested Program Change Due to New Statute Program Change Due to Agency Discretion Change Due to Adjustment in Agency Estimate Change Due to Potential Violation of the PRA Previously Approved
Annual Number of Responses for this IC 139,561 0 0 15,117 0 124,444
Annual IC Time Burden (Hours) 194,349 0 0 22,073 0 172,276
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.
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