Veterinary Feed Directive

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
0363 Veterinary Feed Directive SS for 2015 final rule.pdf	Supporting Statement A	Uploaded 2015-05-19	Available
CVM 2014-376 FRIA VFD.doc	Supplementary Document	Uploaded 2015-05-18	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
5992	Review of VFD Final Rule by affected respondents (one time burden)		Modified
216541	3rd Party: Acknowledgement Letter		New
216540	3rd Party: Issuance of VFD by veterinarian		New
216539	VFD Recordkeeping Requirements by Distributors		New
216535	Notification of business change by distributor		New
216533	Notification of VFD distribution		New

ICR Details

OMB Control No: 0910-0363	ICR Reference No: 201505-0910-001
Status: Historical Active	Previous ICR Reference No: 201412-0910-010
Agency/Subagency: HHS/FDA	Agency Tracking No: CVM
Title: Veterinary Feed Directive
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 07/07/2015
	Date Received in OIRA: 05/19/2015
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	07/31/2018	36 Months From Approved	02/28/2018
Responses	3,019,749	0	2,250,321
Time Burden (Hours)	145,563	0	132,033
Cost Burden (Dollars)	11,584,259	0	0

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Abstract: A VFD drug is a drug intended for use in animal feeds and limited to use under the professional supervision of a licensed veterinarian. This information collection request supports the agency's regulations establishing the requirements for the distribution and use of VFD drugs and animal feeds containing VFD drugs. Respondents to the collection are VFD Feed distributors, veterinarians, and food animal producers.

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Authorizing Statute(s): PL: Pub.L. 104 - 250 5 Name of Law: Animal Drug Availability Act
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
0910-AG95	Final or interim final rulemaking	80 FR 31707	06/03/2015

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	78 FR 75515	12/12/2013
30-day Notice:	Federal Register Citation:	Citation Date:
	78 FR 75515	12/12/2013
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 6

table that charts list of burden

IC Title	Form No.	Form Name
3rd Party: Issuance of VFD by veterinarian
Notification of VFD distribution
Notification of business change by distributor
VFD Recordkeeping Requirements by Distributors
Review of VFD Final Rule by affected respondents (one time burden)
3rd Party: Acknowledgement Letter

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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	3,019,749	2,250,321	0	769,428	0	0
Annual Time Burden (Hours)	145,563	132,033	0	13,530	0	0
Annual Cost Burden (Dollars)	11,584,259	0	0	11,584,259	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Changing Regulations

Burden decreases because of Program Change due to Agency Discretion: Yes

Burden Reduction Due to: Changing Regulations

Short Statement: Previously the information collection provisions supporting the respective regulations were consolidated. Because of the changes in and renumbering of the individual regulations, we are now itemizing certain provisions for ease of reference and greater clarity. These changes are explained more fully in the agency's supporting statement.

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Annual Cost to Federal Government: $1,900

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: 05/19/2015

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