Records and Reports Concerning Experience with Approved New Animal Drugs

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form Form FDA 1932 Veterinary Adverse Drug Reaction; Lack of Effectiveness or Product Defect Report	Form and Instruction	Modified	Available
Form 2301 Transmittal of Periodic reports and Promotional Material	Form and Instruction	Modified	Available
Form 2301 Transmittal of Periodic Reports and Promotional Material forNew Animal Drugs	Form	Modified	Available
Form 2301 Transmittal of Periodic Reports and Promotional Material	Form and Instruction	Modified	Available
Form 2301 Transmittal of Periodic Reports and Promotional Material	Form and Instruction	Modified	Available
Form 1932a Veterinary Adverse Drug Reaction, Lack of Effectiveness	Form and Instruction	Unchanged	Available
0284 OMB Justification Memo for 83C Change Request.doc	Justification for No Material/Nonsubstantive Change	Uploaded 2017-03-10	Repair queued
0284 Supporting Statement 2014.pdf	Supporting Statement A	Uploaded 2014-12-16	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
37624	Records and Reports Concerning Experience with Approved New Animal Drugs	Form and Instruction	Modified	Veterinary Adverse Drug Reaction; Lack of Effectiveness or Product Defect Report
197284	Recordkeeping: Maintainence of Records ( data) by Applicants & Non Applicants That Was Not Submitted as Part of the NADA Application		Unchanged
197283	Reporting: Requirement for submitting Distributor statements - Form FDA 2301	Form and Instruction	Modified	Transmittal of Periodic reports and Promotional Material
197283	Reporting: Requirement for submitting Distributor statements - Form FDA 2301	Other-Screenshots - Proposed Electronic Submitter System	Modified
197282	Reporting: Requirement for Submitting Advertisement & Promotional Material - Form FDA 2301	Form	Modified	Transmittal of Periodic Reports and Promotional Material forNew Animal Drugs
197282	Reporting: Requirement for Submitting Advertisement & Promotional Material - Form FDA 2301	Other-Screenshots - Proposed Electronic Submitter System	Modified
197281	Reporting: Requirement for Submission of Special Drug Experience Report More Frequently - Form FDA 2301	Form and Instruction	Modified	Transmittal of Periodic Reports and Promotional Material
197281	Reporting: Requirement for Submission of Special Drug Experience Report More Frequently - Form FDA 2301	Other-Screenshots - Proposed Electronic Submitter System	Modified
197280	Reporting: Annual drug experience report Form FDA 2301	Form and Instruction	Modified	Transmittal of Periodic Reports and Promotional Material
197280	Reporting: Annual drug experience report Form FDA 2301	Other-Screenshots - Proposed Electronic Submitter System	Modified
197279	Reporting: Adverse Drug Experience & Product / Manufacturing Defects Voluntary reporting Using Form FDa 1932a	Form and Instruction	Unchanged	Veterinary Adverse Drug Reaction, Lack of Effectiveness

ICR Details

OMB Control No: 0910-0284	ICR Reference No: 201703-0910-012
Status: Historical Active	Previous ICR Reference No: 201412-0910-009
Agency/Subagency: HHS/FDA	Agency Tracking No: CVM
Title: Records and Reports Concerning Experience with Approved New Animal Drugs
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 05/05/2017
Retrieve Notice of Action (NOA)	Date Received in OIRA: 03/15/2017
Terms of Clearance: Approved with the understanding that FDA is currently seeking public comment on this collection and revisions may be made to the new electronic submission instrument as part of the upcoming extension request.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	02/28/2018	02/28/2018	02/28/2018
Responses	12,410	0	12,410
Time Burden (Hours)	101,365	0	101,365
Cost Burden (Dollars)	0	0	0

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Abstract: The continuous monitoring of approved New Animal Drug Applications affords the primary means by which FDA obtains information regarding potential problems in safety and effectiveness of marketed animal drugs and potential manufacturing problems. Adverse reaction reports are required to be submitted by the drug manufacturer on FDA forms 1932 and 1932a( voluntary reporting form), following complaints from animal owners or veterinarians . Also product defects and lack of effectiveness complaints are submitted to FDA by the drug manufacturer following their own detection of a problem or complaints from product users or their veterinarians using forms FDA 1932 and 1932a. Form 2301 is used to submit the required transmittal reports and promotional material for new animal drugs.

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Authorizing Statute(s): US Code: 21 USC 512(I)
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 58355	09/29/2014
30-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 74728	12/16/2014
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 7

table that charts list of burden

IC Title	Form No.	Form Name
Recordkeeping: Maintainence of Records ( data) by Applicants & Non Applicants That Was Not Submitted as Part of the NADA Application
Records and Reports Concerning Experience with Approved New Animal Drugs	Form FDA 1932	Veterinary Adverse Drug Reaction; Lack of Effectiveness or Product Defect Report
Reporting: Adverse Drug Experience & Product / Manufacturing Defects Voluntary reporting Using Form FDa 1932a	1932a	Veterinary Adverse Drug Reaction, Lack of Effectiveness
Reporting: Annual drug experience report Form FDA 2301	2301	Transmittal of Periodic Reports and Promotional Material
Reporting: Requirement for Submission of Special Drug Experience Report More Frequently - Form FDA 2301	2301	Transmittal of Periodic Reports and Promotional Material
Reporting: Requirement for Submitting Advertisement & Promotional Material - Form FDA 2301	2301	Transmittal of Periodic Reports and Promotional Material forNew Animal Drugs
Reporting: Requirement for submitting Distributor statements - Form FDA 2301	2301	Transmittal of Periodic reports and Promotional Material

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ICR Summary of Burden

table that charts list of burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	12,410	12,410	0	0	0	0
Annual Time Burden (Hours)	101,365	101,365	0	0	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $700,000

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 03/15/2017

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