Information Collection

Veterinary Adverse Drug Reaction, Lack of Effectivenesss, Product Defect Report, and Transmittal of Periodic Reports and Promotional Material for New Animl Drugs, 21 CFR Part 510

IC 5665 under ICR 200303-0910-006 · OMB 0910-0012.

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Information Collection (IC) Details

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IC Title:

Veterinary Adverse Drug Reaction, Lack of Effectivenesss, Product Defect Report, and Transmittal of Periodic Reports and Promotional Material for New Animl Drugs, 21 CFR Part 510

Agency IC Tracking Number:

Is this a Common Form? No

IC Status: Migrated

Obligation to Respond: Mandatory

CFR Citation:

Information Collection Instruments:

table that charts list of instruments
Document Type	Form No.	Available Electronically?	Can Be Submitted Electronically?
Form	FDA-1932A	No	No
Form	FDA-1932	No	No
Form	FDA-2301	No	No

Federal Enterprise Architecture Business Reference Module

Line of Business:

Subfunction:

Privacy Act System of Records

Title:

FR Citation:

Number of Respondents: 290

Number of Respondents for Small Entity: 0

Affected Public: Private Sector

Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 0 %

table that charts list of burden
	Approved	Change Due to Adjustment in Agency Estimate	Previously Approved
Annual Number of Responses for this IC	20,564	13,814	6,750
Annual IC Time Burden (Hours)	68,621	14,396	54,225
Annual IC Cost Burden (Dollars)	0	0	0

Documents for IC

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Title	Document	Date Uploaded

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

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