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

Documents and Forms

Document Name Document Type

no available documents/forms check other ICs listed under this ICR

Information Collection (IC) Details

View Information Collection (IC)

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:

Document Type	Form No.	Available Electronically?	Can Be Submitted Electronically?
Form	FDA-2301	No	No
Form	FDA-1932A	No	No
Form	FDA-1932	No	No

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 %

	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

Title	Document	Date Uploaded

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