Animal Drug Adverse Event Information Collection Activities

Adverse Experience/Events with Approved New Animal Drugs

OMB: 0910-0284

IC ID: 37624

Documents and Forms

Document Name Document Type
Form FDA 1932 Animal Drug Adverse Event Information Collection Activities Form and Instruction
FDA 1932 VETERINARY ADVERSE DRUG REACTION, LACK OF EFFECTIVENESS, PRODUCT DEFECT REPORT FORM FDA 1932.pdf Form and Instruction
FDA 1932a VETERINARY ADVERSE DRUG REACTION, LACK OF EFFECTIVENESS, OR PRODUCT DEFECT REPORT (voluntary reporting) FORM FDA 1932a.pdf Form and Instruction
FDA 2301 TRANSMITTAL OF PERIODIC REPORTS AND PROMOTIONAL MATERIAL FOR NEW ANIMAL DRUGS FORM FDA 2301.pdf Form and Instruction