AdverseDrug 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⚠️ Notice: This information collection may be referencing outdated material.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 1932a AdverseDrug Experiences & Product /Manufacturing Defects Voluntary Reporting Using Form FDA 1932a Form and Instruction
1932a Veteinay Adverse Drug Reaction Lack of Effectiveness Form FDA 1932a.pdf Form and Instruction

Information Collection (IC) Details

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

Is this a Common Form?		IC Status: New

Obligation to Respond: Voluntary

CFR Citation: 21 CFR 514.80(b)(1) 21 CFR 514.80(b)(2)(i)&(ii) 21 CFR 514.80(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	1932a	Veteinay Adverse Drug Reaction Lack of Effectiveness	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
Annual Number of Responses for this IC	82	82
Annual IC Time Burden (Hours)	82	82
Annual IC Cost Burden (Dollars)	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.