Reporting: Adverse Drug Experience & Product / Manufacturing Defects Voluntary reporting Using Form FDa 1932a

Records and Reports Concerning Experience with Approved New Animal Drugs

OMB: 0910-0284

IC ID: 197279

Information Collection (IC) Details

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Reporting: Adverse Drug Experience & Product / Manufacturing Defects Voluntary reporting Using Form FDa 1932a
 
No Unchanged
 
Voluntary
 
21 CFR 514.80(b)1;(b)2;&(b)3

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Form and Instruction 1932a Veterinary Adverse Drug Reaction, Lack of Effectiveness Form FDA 1932a.pdf Yes Yes Fillable Printable

Health Consumer Health and Safety

 

197 0
   
Private Sector Businesses or other for-profits
 
   0 %

  Approved 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 197 0 0 0 0 197
Annual IC Time Burden (Hours) 197 0 0 0 0 197
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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