Adverse Drug Experiences & Product / Manufacturing Defects Voluntary Reporting Using Form FDA 1932a

Records and Reports Concerning Experience with Approved New Animal Drugs

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0284 can be found here:

Documents and Forms

Document Name Document Type
Form 1932 A Adverse Drug Experiences & Product / Manufacturing Defects Voluntary Reporting Using Form FDA 1932a Form and Instruction
1932 A Veterinary Adverse Drug Reaction, Lack of Effectiveness Form FDA 1932a.pdf Form and Instruction

Information Collection (IC) Details

IC Title:	Adverse Drug Experiences & Product / Manufacturing Defects Voluntary Reporting Using Form FDA 1932a	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: New

Obligation to Respond: Voluntary

CFR Citation: 21 CFR 514.80(b)1;(b)2;(b)3

Information Collection Instruments:

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

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 82	Number of Respondents for Small Entity: 0

Affected Public: Private Sector	Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 0 %

	Requested	Program Change Due to Agency Discretion	Change Due to Potential Violation of the PRA
Annual Number of Responses for this IC	82	-43,436	43,518
Annual IC Time Burden (Hours)	82	-83,473	83,555
Annual IC Cost Burden (Dollars)	0	0	0

Documents for IC

Title	Document	Date Uploaded
No associated records found

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